A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance

✍ Scribed by Gianina Ravenscroft; Jo M. Wilmshurst; Komala Pillay; Padma Sivadorai; William Wallefeld; Kristen J. Nowak; Nigel G. Laing

• Book ID: 116794707
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 981 KB
• Volume: 21
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2010.08.005