A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease

  • Patrick J. Lynch
  • , Jiefei Tong
  • , Mary Lehane
  • , Alejandro Mallet
  • , Linda Giblin
  • , James J.A. Heffron
  • , Pat Vaughan
  • , Gildardo Zafra
  • , David H. MacLennan
  • , Tommie V. McCarthy

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology