Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin

✍ Scribed by Katharine Forrest; Jemima E. Mellerio; Stephanie Robb; Patricia J.C. Dopping-Hepenstal; John A. McGrath; Lu Liu; Stefan J.A. Buk; Safa Al-Sarraj; Elizabeth Wraige; Heinz Jungbluth

• Book ID: 116794420
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 288 KB
• Volume: 20
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2010.06.003