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night blindness, congenital stationary (incomplete)
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CACNA1F
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
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MAPK signaling pathway
Homo sapiens (human)
one gene
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