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Qaagi - Book of Why

Causes

Effects

Mutations in cornea- specific keratins K3 or K12 genescauseMeesmann corneal dystrophy

CrossRef ] [ PubMed ] Irvine AD Corden LD Swensson O Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

1997 ) Mutations in cornea‐specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

Pubmed ] Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

the opacityresultingfrom a corneal dystrophy

L Corden Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

Aldave A. UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

Schnyder UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

2010 ) UBIAD1 Mutation Alters a Mitochondrial Prenyltransferaseto CauseSchnyder Corneal Dystrophy

2011 UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

McLean , W.H. Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

Jayne S Weiss UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

09 - 12 UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

Lu W. UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

intense signal neurontin onset time Mutations in cornea - specific keratin K3 of K12 genescauseMeesmannвs corneal dystrophy

dominant negative mutations in cornea - specific keratins K3 or K12(passive) is caused byMeesmann 's corneal dystrophy

Full Text Novel mutation in the CHST6 genecausesmacular corneal dystrophy

Pras E. Novel mutation in the CHST6 genecausesmacular corneal dystrophy

et al Novel mutations in the CHST6 genecausingmacular corneal dystrophy

Ref.15"Novel mutations in the CHST6 genecausingmacular corneal dystrophy

Number to send5102050100200Start from citationCreate File Select item 91718311.Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

Irvine AD , Corden LD , Swensson Ayyia , et al Mutations in cornea - specific keratin K3 or K12 genescauseMeesmannвs corneal dystrophy

OX=9606 GN = KRT3 PE=1 SV=3 " Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

2008;40:105 - 8 pubmed publisher Abbruzzese C , Kuhn U , Molina F , Rama P , De Luca M. Novel mutations in the CHST6 genecausingmacular corneal dystrophy

10.1371 / journal.pone.0010760.UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeSchnyder corneal dystrophy

pmid ' : 9171831 , ' year ' : 1997 , ' title ' : " Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

15737194 [ PubMed - indexed for MEDLINE ] Free ArticleRelated citations Select item 91718316.Mutations in cornea - specific keratin K3 or K12 genescauseMeesmann 's corneal dystrophy

mutations in the KRT12 gene(passive) caused byMeesmann corneal dystrophy

the spectrum of mutations in the CHST6 genecausemacular corneal dystrophy

association of 2 mutations in the TGFBI gene - R124L and deltaT125-deltaE126."Dighiero P. , Drunat S. , D'Hermies F. , Renard G. , Delpech M.(passive) caused bygranular corneal dystrophy

association of 2 mutations in the TGFBI gene — R124L and ΔT125-ΔE126(passive) caused bygranular corneal dystrophy

arvojournals.org ) Mutations in the gene encoding this proteinleadto Meesmann corneal dystrophy

new mutation in UBIAD1 genecausesSchnyder corneal dystrophy

mutations in cornea - specific keratins " , author(passive) is caused byMeesmann 's corneal dystrophy

17668063 ) Mutations in the UBIAD1 gene on chromosome short arm 1 , region 36causeSchnyder crystalline corneal dystrophy

datA Deletion of the Felipe Molina , Kirsten Novel mutations in the CHST6 genecausingmacular corneal dystrophy

mutations in the DCN gene Where is the DCN gene located(passive) caused bycongenital stromal corneal dystrophy

Peter S White Article : Mutations in the UBIAD1 gene on chromosome short arm 1 , region 36causeSchnyder crystalline corneal dystrophy

View at Scopus M. L. Nickerson , B. N. Kostiha , W. Brandt et al . , “ UBIAD1 mutation alters a mitochondrial prenyltransferaseto causeschnyder corneal dystrophy

3 4 22 58 Mutations in the UBIAD1 gene on chromosome short arm 1 , region 36causeSchnyder crystalline corneal dystrophy

the cornea to lose its clarity , with the result being decreased or blurred visioncan causethe cornea to lose its clarity , with the result being decreased or blurred vision

following LASIKdiscoveredfollowing LASIK

the surrounding Suboptimal vision(passive) caused bythe surrounding Suboptimal vision

from an R124H Big - h3 mutation after phototherapeutic keratectomy 5resultingfrom an R124H Big - h3 mutation after phototherapeutic keratectomy 5

from an R124H Big - h3 mutation after phototherapeutic keratectomy 2resultingfrom an R124H Big - h3 mutation after phototherapeutic keratectomy 2

from betaig - h3 R124H mutationresultingfrom betaig - h3 R124H mutation

from kerato - epithelin mutations at Arg-124resultingfrom kerato - epithelin mutations at Arg-124

from homozygous and heterozygous R124H BIG - H3 mutationresultingfrom homozygous and heterozygous R124H BIG - H3 mutation

cloudiness in the corneacausescloudiness in the cornea

a hazy opacity of the eyecreatesa hazy opacity of the eye

opacification of the cornea which leads to loss of visioncausesopacification of the cornea which leads to loss of vision

significant vision problems and even blindnesscan causesignificant vision problems and even blindness

in the formation of opaque Cholesterol deposits within the eye , and sure breeds of canine are more vulnerable to this situation than otherscan resultin the formation of opaque Cholesterol deposits within the eye , and sure breeds of canine are more vulnerable to this situation than others

to the formation of opaque Cholesterol deposits within the eye , and certain breeds of canine are more susceptible to this condition than otherscan leadto the formation of opaque Cholesterol deposits within the eye , and certain breeds of canine are more susceptible to this condition than others

in blindness or corneal ulcerationmay resultin blindness or corneal ulceration

no problems , moderate vision impairment , or severe difficulties that require surgerymay ... causeno problems , moderate vision impairment , or severe difficulties that require surgery

to vision loss after laser eye surgerycan leadto vision loss after laser eye surgery

to vision loss after laser eye surgery5can leadto vision loss after laser eye surgery5

secondary corneal erosions , with photophobia and painoften causessecondary corneal erosions , with photophobia and pain

from a Big - h3 R124H mutation"British Journal of Ophthalmologyresultingfrom a Big - h3 R124H mutation"British Journal of Ophthalmology

from a Big - h3 R124H mutation"British Journal of Ophthamlologyresultingfrom a Big - h3 R124H mutation"British Journal of Ophthamlology

to the formation of opaque Cholesterol deposits in the eye , and sure breeds of dog are extra liable to this situation than otherscan leadto the formation of opaque Cholesterol deposits in the eye , and sure breeds of dog are extra liable to this situation than others

2 Corneal endothelial dystrophy 3 Commonly affected breeds Suboptimal vision(passive) caused by2 Corneal endothelial dystrophy 3 Commonly affected breeds Suboptimal vision

The progressive loss of vision(passive) caused byThe progressive loss of vision

in vision loss after lasek5can resultin vision loss after lasek5

to the formation of opaque Cholesterol deposits in the eye , and certain breeds of dog Cholesterol spots are extra prone to this condition than otherscan leadto the formation of opaque Cholesterol deposits in the eye , and certain breeds of dog Cholesterol spots are extra prone to this condition than others

degeneration of the cornea rather unpredictablycausesdegeneration of the cornea rather unpredictably

to the progressive thinning of the center of cornealeadsto the progressive thinning of the center of cornea

to the outer layer of the cornea detaching ... causing pain and vision lossleadsto the outer layer of the cornea detaching ... causing pain and vision loss

to repeated superficial corneal erosions that take longer to healcan leadto repeated superficial corneal erosions that take longer to heal

dry eye and blurry visionmost likely causingdry eye and blurry vision

lipids to build up in the outer transparent surface of the eye known as the corneacauseslipids to build up in the outer transparent surface of the eye known as the cornea

the cornea to lose its clarity , with the result being decreasecan causethe cornea to lose its clarity , with the result being decrease

the appearance of spots on the surface ( cornea ) of the eyecausesthe appearance of spots on the surface ( cornea ) of the eye

white or gray localized lesions to appear in the corneacauseswhite or gray localized lesions to appear in the cornea

abnormal thinning and an atypical cone shape of the corneacausesabnormal thinning and an atypical cone shape of the cornea

blurry vision and vision loss if not treated earlycausesblurry vision and vision loss if not treated early

the clear outer covering of the eye ( the cornea ) to become cloudycausesthe clear outer covering of the eye ( the cornea ) to become cloudy

to pain and swelling of the eye as well as significant vision lossleadto pain and swelling of the eye as well as significant vision loss

from a βig - h3 R124H mutation | British Journal of Ophthalmology Corneal guttata associated with the corneal dystrophy resulting from a βig - h3 R124H mutationresultingfrom a βig - h3 R124H mutation | British Journal of Ophthalmology Corneal guttata associated with the corneal dystrophy resulting from a βig - h3 R124H mutation

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