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Smart Reasoning:

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Qaagi - Book of Why

Causes

Effects

by mutations the USH2A gene(passive) is caused byUsher syndrome type 2A

Mutation of cdh23 , encoding a new member of the cadherin gene familycausesusher syndrome type 1d

Mutation of CDH23 , encoding a new member of the cadherin gene familycausesUsher syndrome type

Mutations in at least six genescan causeUsher syndrome type

a nonsense mutationcausingUsher syndrome type

A mutation , ... , the leading genetic cause of combined deafness and blindnesscauseshuman Usher syndrome

by mutations in one of several different genes(passive) can be caused byUsher syndrome type I. Usher syndrome type

myosin VIIa mutationscausingUsher syndrome type

myosin VIIacauseUsher syndrome type

Currently twelve genescausingUsher syndrome types

a genetic mutation(passive) is caused byCauses Usher syndrome

mutation in the USH2A gene(passive) is caused byUsher syndrome 2A

by a mutation in MYO7A.(passive) caused byUsher syndrome 1B

A mutation in any one of these genes ... likelyto resultin Usher syndrome

the genecausesAcadian Usher Syndrome

its enzymatic activitycausingatypical Usher syndrome

by mutations in a number of genes(passive) is caused byUsher syndrome

by a mutation in several genes(passive) can be caused byUsher syndrome

Mutations in several different genes have been foundto causeUsher syndrome

a mutation in the Ush1c gene , the same genecausesUsher syndrome

any known mutationsleadingto Usher syndrome

mutations in any of more than ten genes(passive) is caused byUsher syndrome

people with USH2A mutationscausingUsher syndrome

mutations in several different genes(passive) can be caused byUsher syndrome

the mutation of genes(passive) is caused byUsher Syndrome

Mutations in the CDH23 , CLRN1 , GPR98 , MYO7A , PCDH15 , USH1C , USH1 G , and USH2A genescauseUsher syndrome

more than one genecausesUsher syndrome

by mutations in MYO7A or USH2A(passive) caused byUsher syndrome

two novel frameshift mutations in GPR98 ( Table 2 ... knownto causeUsher syndrome

At least 13 genes are knownto causeUsher syndrome

by homozygous mutations of Ush2a(passive) caused byUsher syndrome

a mutation in any one of thencan causeUsher syndrome

specific mutationsresultin Usher syndrome

by USH2A mutations(passive) caused byUsher syndrome

USH2A mutationscausingUsher syndrome

mutations in USH2Acan ... causeUsher syndrome

different mutationscan causeUsher syndrome

different mutationscauseUsher syndrome , and

whose mutationscan causeUsher Syndrome

mutations in DNA(passive) is caused byUsher syndrome

in impairment of both hearing and vision , as well as balanceresultsin impairment of both hearing and vision , as well as balance

both Deafness and blindnesscausesboth Deafness and blindness

in blindness and deafnessresultsin blindness and deafness

hearing loss and gradual loss of visioncauseshearing loss and gradual loss of vision

in hearing and eye sightresultingin hearing and eye sight

hearing and vision losscauseshearing and vision loss

deafness and blindnesscan causedeafness and blindness

a gradual loss of vision and hearing over time due to abnormalities found within the ears and eyescausesa gradual loss of vision and hearing over time due to abnormalities found within the ears and eyes

him to go blindwill causehim to go blind

in him having a hearing impairmenthas resultedin him having a hearing impairment

hearing loss early in life and vision loss beginning in adolescence or young adulthoodcauseshearing loss early in life and vision loss beginning in adolescence or young adulthood

retinitis pigmentosacan causeretinitis pigmentosa

deafness and blindnesscausesdeafness and blindness

progressive loss of visioncausesprogressive loss of vision

for examplecausesfor example

a loss of vision and hearingcausesa loss of vision and hearing

deafness or hearing impairment at birth and vision impairment later in lifecausesdeafness or hearing impairment at birth and vision impairment later in life

up your own patient filesettingup your own patient file

deafblindnesscausesdeafblindness

children to be born with severe to profound hearing losscauseschildren to be born with severe to profound hearing loss

in congenital deafness , vestibular dysfunction , and blindnessresultsin congenital deafness , vestibular dysfunction , and blindness

in deafness and vision lossresultsin deafness and vision loss

him to be hard of hearingcausedhim to be hard of hearing

to progressive hearing and vision lossleadsto progressive hearing and vision loss

genescausinggenes

her hearing and sight to slowly disappearhas causesher hearing and sight to slowly disappear

him to lose his hearingcausedhim to lose his hearing

deafness and progressive degeneration of the retina ... leading to blindnesscausesdeafness and progressive degeneration of the retina ... leading to blindness

in acute deafness at birth and then a gradual loss of visionresultsin acute deafness at birth and then a gradual loss of vision

both hearing loss and vision loss due to retinitis pigmentosacausesboth hearing loss and vision loss due to retinitis pigmentosa

deafness and blindness due to genetic defects in the Usher genecausesdeafness and blindness due to genetic defects in the Usher gene

in hearing loss and vision loss due to retinitis pigmentosa ( RPusually resultsin hearing loss and vision loss due to retinitis pigmentosa ( RP

hearing loss or deafness at birthcauseshearing loss or deafness at birth

hearing loss but is also associated with vision losscauseshearing loss but is also associated with vision loss

progressive sight and hearing losscausesprogressive sight and hearing loss

blindness due to retinitis pigmentosacausesblindness due to retinitis pigmentosa

in acute deafness at birthresultsin acute deafness at birth

deafness and progressive degeneration of the retinacausesdeafness and progressive degeneration of the retina

deafness and progressive degeneration of the retinacausesdeafness and progressive degeneration of the retina

deafness and blindnesscausesdeafness and blindness

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