Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome (Q35447613)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome |
scientific article |
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Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome (English)
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R E Amir
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P Fang
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Z Yu
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D G Glaze
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A K Percy
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B B Roa
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I B Van den Veyver
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1 February 2005
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42
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2
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e15
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