Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease
Brain. 2012 Aug;135(Pt 8):e217, 1-6; author reply e218, 1-2.
doi: 10.1093/brain/aws034.
Epub 2012 Mar 1.
No abstract available
Publication types
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Letter
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Research Support, Non-U.S. Gov't
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Comment
MeSH terms
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Female
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Hereditary Central Nervous System Demyelinating Diseases / genetics*
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Humans
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Male
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Mutation*
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Myelin Proteins / genetics*