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C.O.7 Cap disease associated with mutations in the β-tropomyosin gene (TPM2)

✍ Scribed by M. Ohlsson; H. Tajsharghi; C. Lindberg; E. Lacène; A. Oldfors; M. Fardeau

Book ID: 116793309
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 46 KB
Volume: 17
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2007.06.462

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