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A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot–Marie–Tooth disease with irregularly folded myelin sheaths

✍ Scribed by Eva Nelis; Sevim Erdem; Ersin Tan; Ann Löfgren; Chantal Ceuterick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman; Haluk Topaloglu

Book ID: 117669579
Publisher: Elsevier Science
Year: 2002
Tongue: English
Weight: 258 KB
Volume: 12
Category: Article
ISSN: 0960-8966
DOI: 10.1016/s0960-8966(02)00046-9

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