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.