(Q40844314)
Statements
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An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor (English)
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Monnier N
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Romero NB
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Lerale J
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Nivoche Y
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Qi D
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MacLennan DH
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Fardeau M
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Lunardi J
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1 November 2000
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9
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18
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2599-2608
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Identifiers
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