Associated Papers
Mutation screening in autosomal dominant congenital cataract families from North India.
Goyal S et al.
Molecular Genetics and Genomics : Mgg, 2023
Screening the pathogenic causes of congenital cataract via whole exome sequencing technology in three families: Molecular genetics of congenital cataract.
Qi C et al.
Molecular Medicine Reports, 2023
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.
Irum B et al.
Human Genome Variation, 2022
36075891 (PubMed )
Supplement: 41439_2022_208_MOESM1_ESM.pdf
Molecular and structural analysis of genetic variations in congenital cataract.
Kumar M et al.
Molecular Vision, 2013
Autosomal-dominant cerulean cataract in a chinese family associated with gene conversion mutation in beta-B2-crystallin.
Wang L et al.
Ophthalmic Research, 2009
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