Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene - Concepedia

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Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

115

Citations

33

References

2007

Year

Heinz Jungbluth, Haiyan Zhou, Caroline A. Sewry, S. Robb, Susan Treves, Marc Bitoun, Pascale Guicheney, Anna Buj‐Bello, Carsten G. Bönnemann, Francesco Muntoni

Neuromuscular Disorders

Muscle FunctionSkeletal MuscleMedicineGeneticsMolecular BiologyDominant MutationNeuromuscular PathologyCentronuclear Myopathy

References

	Year	Citations

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