An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene

✍ Scribed by Burcu Balci; Gökhan Uyanik; Pervin Dincer; Claudia Gross; Tobias Willer; Beril Talim; Göknur Haliloglu; Gülsev Kale; Ute Hehr; Jürgen Winkler; Haluk Topaloğlu

• Book ID: 116792301
• Publisher: Elsevier Science
• Year: 2005
• Tongue: English
• Weight: 230 KB
• Volume: 15
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2005.01.013