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C.O.1 Identification of a new gene mutated in autosomal recessive centronuclear myopathy, and functional links with the dominant form

✍ Scribed by A. Nicot; A. Toussaint; V. Tosch; C. Kretz; C. Wallgren-Pettersson; E. Iwarsson; H. Kingston; J. Garnier; V. Biancalana; J. Mandel; J. Laporte

Book ID: 116793091
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 51 KB
Volume: 17
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2007.06.242

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