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24. Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. Jungbluth H; Zhou H; Sewry CA; Robb S; Treves S; Bitoun M; Guicheney P; Buj-Bello A; Bönnemann C; Muntoni F Neuromuscul Disord; 2007 Apr; 17(4):338-45. PubMed ID: 17376685 [TBL] [Abstract][Full Text] [Related]
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