Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry. (Q48881167)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry. |
scientific article |
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Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry. (English)
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R Herrmann
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V Straub
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K Meyer
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T Kahn
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M Wagner
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T Voit
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1 November 1996
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155
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11
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968-976
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