QuickView for CRYBB3;jsessionid=0BBB57BA576FC564A7BB641E08AF8D89;jsessionid=D25758D919E07DFA4DF916A463FE50A4 (gene)

1. A Novel CRYBB2 Silent Variant in Autosomal Dominant Congenital Cataracts (ADCC) in Pakistani familie…
2. A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital ca…
3. Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.
4. Whole-exome sequencing identification of a recurrent CRYBB2 variant in a four-generation Chinese fam…
5. Polymorphisms in CRYBB2 encoding βB2-crystallin are associated with antisaccade performance and memo…

There were no clinical trials for CRYBB3;jsessionid=0BBB57BA576FC564A7BB641E08AF8D89;jsessionid=D25758D919E07DFA4DF916A463FE50A4