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
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 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
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