Proximal myotonic dystrophy—a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?

✍ Scribed by Bjarne Udd; Ralf Krahe; Carina Wallgren-Pettersson; Björn Falck; Hannu Kalimo

• Book ID: 117670599
• Publisher: Elsevier Science
• Year: 1997
• Tongue: English
• Weight: 814 KB
• Volume: 7
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/s0960-8966(97)00041-2