A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene (Q39003495)

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scientific article published on June 2002
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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene
scientific article published on June 2002

    Statements

    A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene (English)
    Carsten Bönnemann
    Charles-Antoine Haenggeli
    Heinz Jungbluth
    Arnaud Lemainque
    Pascale Guicheney

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