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Null mutations causing depletion of the type 1 ryanodine rec…
Null mutations causing depletion of the type 1 ryanodine receptor %28RYR1%29 are commonly associated with recessive structural congenital myopathies with cores.
Null mutations causing depletion of the type 1 ryanodine receptor %28RYR1%29 are commonly associated with recessive structural congenital myopathies with cores.
Article, Chapter
Authors: N. Monnier
Publication: Human Mutation, Volume:29, Issue:5, Page(s):-678
Published: Wiley, 2008
ISSN: 1059-7794
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