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PNAS.96.7.4164
PNAS.96.7.4164
http://dx.doi.org/10.1073/PNAS.96.7.4164
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.
P356
Q36460971-7DF152E2-E310-4AD1-A987-77EAF13BA43F
P356
PNAS.96.7.4164
http://dx.doi.org/10.1073/PNAS.96.7.4164