Congenital hypomyelinating neuropathy due to de novo heterozygous p. Asp6lAsn MPZ mutation: heterogeneous phenotypes caused by a single mutation in MPZ gene
書誌事項
- タイトル
- Congenital hypomyelinating neuropathy due to de novo heterozygous p. Asp6lAsn MPZ mutation: heterogeneous phenotypes caused by a single mutation in MPZ gene
- 著者
- Yonekawa T, Saito Y
収録刊行物
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- Pediatric Neurology
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Pediatric Neurology 59-21, 2013
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詳細情報
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- CRID
- 1010282257101583622
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- 資料種別
- journal article
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- データソース種別
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- KAKEN