Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

✍ Scribed by Helbling-Leclerc, Anne; Zhang, Xu; Topaloglu, Haluk; Cruaud, Corinne; Tesson, Frédérique; Weissenbach, Jean; Tomé, Fernando M.S.; Schwartz, Ketty; Fardeau, Michel; Tryggvason, Karl

• Book ID: 109918279
• Publisher: Nature Publishing Group
• Year: 1995
• Tongue: English
• Weight: 315 KB
• Volume: 11
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng1095-216