IndraLab

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EAF2 activates CACNA1F. 1 / 1
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"Congenital stationary night blindness (CSNB) is a heterogeneous group of retinal dysfunction caused by autosomal traits (13 recessively inherited genes, 3 dominantly inherited genes) and X linked traits (NYX and CACNA1F) [XREF_BIBR]."