NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia (Q57419078)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia |
No description defined |
Statements
NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia (English)
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2006
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21
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9
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1531-1533
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