A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease (Q36460971)
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Current Data About A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease
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(P1476) "A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease" (language: en)
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(P2093) Lynch PJ
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Tong J
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Lehane M
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Mallet A
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Giblin L
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Heffron JJ
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Vaughan P
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Zafra G
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MacLennan DH
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McCarthy TV
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