Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

Author： Monnier N.

Publisher： Oxford University Press

E-ISSN： 0964-6906|10|22|2581-2592

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.10, Iss.22, 2001-10, pp. : 2581-2592

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