Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, αB-crystallin, myotilin, LMNA or SEPN1 genes

✍ Scribed by Anna Kostera-Pruszczyk; Bertrand Goudeau; Ana Ferreiro; Pascal Richard; Stéphanie Simon; Patrick Vicart; Anna Fidzianska

• Book ID: 116792741
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 412 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2006.07.025