Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. (Q44075701)

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Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.
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    Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. (English)
    Halliger-Keller B

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