Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2. (Q46419617)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2. |
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Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2. (English)
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Carolyn I Hope
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Dianne M Sharp
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Ariana Hemara-Wahanui
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Jennifer I Sissingh
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Patricia Lundon
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Ed A Mitchell
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Marion A Maw
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Gillian M Clover
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1 April 2005
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33
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129-136
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