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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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness |
scientific article |
Statements
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness (English)
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July 1998
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19
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3
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264-7
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