Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
Heinz Jungbluth, Suzanne Lillis, Haiyan Zhou, Stephen Abbs, Caroline Sewry, Michael Swash, Francesco MuntoniVolume:
19
Year:
2009
Language:
english
DOI:
10.1016/j.nmd.2009.02.005
File:
PDF, 338 KB
english, 2009