Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

✍ Scribed by Heinz Jungbluth; Suzanne Lillis; Haiyan Zhou; Stephen Abbs; Caroline Sewry; Michael Swash; Francesco Muntoni

• Book ID: 116793874
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 338 KB
• Volume: 19
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2009.02.005