Late-Onset Axial Myopathy with Cores Due to a Novel Heterozygous Dominant Mutation in the Skeletal Muscle Ryanodine Receptor (Ryr1) Gene

AuthID
 P-00H-CK5
7
Author(s)
Jungbluth H.
·
Lillis S.
·
Zhou H.
·
Abbs S.
·
Sewry C.
·
Muntoni F.
Document Type
Article
Year published
2009
Published
in Neuromuscular Disorders, ISSN: 09608966
Volume: 19, Issue: 5, Pages: 344-347 (3)
Indexing
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 19303294
Scopus: 2-s2.0-67349228165
Source Identifiers
ISSN: 09608966
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