Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in theFKRPgene presenting as acute virus-associated myositis in infancy

✍ Scribed by Maja von der Hagen; Angela M. Kaindl; Kathrin Koehler; Petra Mitzscherling; Hans-Jürgen Häusler; Gisela Stoltenburg-Didinger; Angela Huebner

• Publisher: Springer
• Year: 2005
• Tongue: English
• Weight: 174 KB
• Volume: 165
• Category: Article
• ISSN: 0340-6997
• DOI: 10.1007/s00431-005-1752-6