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- ... Cav1.4 Cav1.4alpha1 COD3 COD4 CORDX CORDX3 CSNB2 CSNB2A CSNBX2 JM8 JMC8 OA2 Tests of CACNA1F ... novel mutation in CACNA1F, the gene responsible for CSNB2. Clin Exp Ophthalmol. 2005 Apr;33(2):129- ...
- X-linked congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light and ...