Condition: Cataract, Congenital Nuclear, Autosomal Recessive 2
rs587777601
in
CRYBB3
gene and
Cataract, Congenital Nuclear, Autosomal Recessive 2
PMID 23508780
2013 Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.
PMID 15914629
2005 Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.