(Q46080022)
Statements
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Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene (English)
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Francesco Muntoni
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Suzanne Lillis
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Haiyan Zhou
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Stephen Abbs
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Caroline Sewry
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19 March 2009
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19
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5
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344-347
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