(Q43800108)
Statements
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Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of 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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Landrieu P
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Nivoche Y
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Fardeau M
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Lunardi J
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1 October 2001
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10
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22
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2581-2592
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Identifiers
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