Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26). (Q33909489)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26). |
scientific article |
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Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26). (English)
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Miquel Tuson
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Roser Gonzàlez-Duarte
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16 December 2003
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74
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128-138
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