O7-4 Kelch-like homolog 9 (KLHL9) mutation is associated with an early onset autosomal dominant distal myopathy

✍ Scribed by S. Cirak; F.V. Deimling; S. Sachdev; W.J. Errington; R. Herrmann; G. Osee; C. Böonnemann; K. Brockmann; S. Hinderlich; T.H. Lindner; A. Steinbrecher; G.G. Prive; M. Hannink; P. Nürnberg; T. Voit

• Book ID: 114359859
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 45 KB
• Volume: 13
• Category: Article
• ISSN: 1090-3798
• DOI: 10.1016/s1090-3798(09)70049-2