P.P.1 01 Congenital muscular dystrophy with mental retradation due to a homozygous protein-o-mannosyltransferase 2 (POMT2) mutation: A case report

✍ Scribed by P.Y.K. Van den Bergh; C. Bouchet; S. Maugenre; A. Yanagisawa; G. Cosnard; F. Leturcq; N. Deburgrave; N. Séta; P. Guicheney

• Book ID: 116792527
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 49 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2006.05.070