Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness (Q24315607)
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Current Data About Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
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(P1476) "Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness" (language: en)

(P2093) N T Bech-Hansen
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M J Naylor
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T A Maybaum
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W G Pearce
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G A Fishman
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M Mets
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M A Musarella
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K M Boycott
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External Links
(P356) 10.1038/947
(P698) 9662400
(P3181) 948727
(P6179) 1009938043