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Autosomal dominant nemaline myopathy caused by a novel α-tropomyosin 3 mutation

✍ Scribed by I. C. Kiphuth; S. Krause; H. B. Huttner; G. Dekomien; T. Struffert; R. Schröder

Book ID: 106094726
Publisher: Springer
Year: 2009
Tongue: English
Weight: 246 KB
Volume: 257
Category: Article
ISSN: 0340-5354
DOI: 10.1007/s00415-009-5413-y

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