G.P.1.02 Phenotypic spectrum of core-rod myopathy caused by dominant or recessive RYR1 mutations

✍ Scribed by K.G. Claeys; N. Monnier; P. Laforet; G. Brochier; A. Ferreiro; A. Barois; B. Eymard; J. Lunardi; M. Fardeau; N.B. Romero

• Book ID: 116793951
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 44 KB
• Volume: 19
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2009.06.044