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.
Article, Chapter
Authors:
N. Monnier
Publication:
Volume:29,
Page(s):670
Published:
2008
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