Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene

✍ Scribed by Jorieke E.H. Bergman; Hermine E. Veenstra-Knol; Anthonie J. van Essen; Conny M.A. van Ravenswaaij; Wilfred F.A. den Dunnen; Arthur van den Wijngaard; J. Peter van Tintelen

• Book ID: 116433047
• Publisher: Elsevier Science
• Year: 2007
• Tongue: English
• Weight: 929 KB
• Volume: 50
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2007.06.003