Hereditary Inclusion Body Myopathy

• मुख्य लेखक: J Gordon Millichap (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Pediatric Neurology Briefs Publishers, 1998-09-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

A new familial, autosomal dominant, myopathy and variant of hereditary inclusion body myopathy (HIBM) is described in 19 members of a large Swedish family followed in the Departments of Pediatrics, Genetics, and Pathology, Sahlgrenska University Hospital, Goteborg, Sweden.