C.P.18 Skeletal muscle myopathy mutations at the actin tropomyosin interface that cause gain or loss of function

✍ Scribed by Memo, M.; Clarke, N.F.; Laing, N.G.; Nowak, K.J.; Ravenscroft, G.; Sewry, C.; Jain, R.; Jayawant, S.; Lehtokari, V.L.; Marttila, M.; Wallgren-Pettersson, C.; Marston, S.B.

• Book ID: 119333772
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 48 KB
• Volume: 22
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2012.06.146