MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin (Q24533455)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin |
scientific article |
Statements
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin (English)
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May 2001
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68
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5
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1093-101
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2 references
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1 reference