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UnknownScreening of CYP1B1 Arg368His as predominant mutation in North Indian primary open angle glaucoma and juvenile onset glaucoma patients.
Not available
S-EPMC6363938 | biostudies-literature
UnknownNovel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
Not available
S-EPMC2650718 | biostudies-literature
UnknownA novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.
Not available
S-EPMC2768755 | biostudies-literature
UnknownGenetics of diabetes.
Not available
S-EPMC10294065 | biostudies-literature
UnknownA nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India.
Not available
S-EPMC10173570 | biostudies-literature
UnknownMolecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in GJA8 and GJA3.
Not available
S-EPMC9755747 | biostudies-literature
UnknownNovel and known variants in GJA3 and LIM2 in congenital cataract families from North India.
Not available
S-EPMC10765620 | biostudies-literature
UnknownA novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
Not available
S-EPMC2255026 | biostudies-literature
UnknownA mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
Not available
S-EPMC2435161 | biostudies-literature
UnknownClinical and molecular aspects of congenital aniridia - A review of current concepts.
Not available
S-EPMC9426064 | biostudies-literature
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