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Title
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Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores
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Author
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Language
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English
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Source (journal)
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Human mutation. - New York, N.Y.
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Publication
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New York, N.Y.
:
2008
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ISSN
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1059-7794
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DOI
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10.1002/HUMU.20696
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Volume/pages
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29
:5
(2008)
, p. 670-678
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ISI
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000255385800012
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Note
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doi:10.1002/humu.20696
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Full text (Publisher's DOI)
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