A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. (Q35592909)
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scientific article published on February 2005
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. |
scientific article published on February 2005 |
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A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. (English)
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M Michaelides
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G E Holder
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D M Hunt
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F W Fitzke
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A C Bird
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A T Moore
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1 February 2005
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89
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2
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198-206
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