Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: Clinical and pathological variability within a kindred

✍ Scribed by David O. Hutchinson; Amanda Charlton; Nigel G. Laing; Biljana Ilkovski; Kathryn N. North

• Book ID: 116792394
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 398 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2005.11.004