DOI:
10.1055/s-00000041
Neuropediatrics
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References
Jungbluth H, Zhou H, Sewry CA. , et al.
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene.
Neuromuscul Disord 2007;
17 (04) 338-345
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