Congenital hypomyelinating neuropathy due to de novo heterozygous p. Asp6lAsn MPZ mutation: heterogeneous phenotypes caused by a single mutation in MPZ gene
Bibliographic Information
- Title
- Congenital hypomyelinating neuropathy due to de novo heterozygous p. Asp6lAsn MPZ mutation: heterogeneous phenotypes caused by a single mutation in MPZ gene
- Author
- Yonekawa T, Saito Y
Journal
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- Pediatric Neurology
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Pediatric Neurology 59-21, 2013
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Details 詳細情報について
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- CRID
- 1010282257101583622
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- Article Type
- journal article
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- Data Source
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- KAKEN