(Q39003495)
Statements
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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 (English)
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Volker Straub
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Michel Fardeau
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Ana Ferreiro
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Nicole Monnier
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Norma B Romero
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Jean-Paul Leroy
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Carsten Bönnemann
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Charles-Antoine Haenggeli
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Wolfgang D Voss
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Yves Nivoche
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Heinz Jungbluth
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Arnaud Lemainque
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Thomas Voit
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Joël Lunardi
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Pascale Guicheney
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1 June 2002
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51
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6
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750-759
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Identifiers
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