Minicore Myopathy with Ophthalmoplegia Caused by Mutations in the Ryanodine Receptor Type 1 Gene

AuthID
 P-015-ASM
16
Author(s)
Jungbluth H.
·
Zhou H.
·
Hartley L.
·
Halliger-Keller B.
·
Messina S.
·
Longman C.
·
Brockington M.
·
Robb S.A.
·
Straub V.
·
Voit T.
·
Ferreiro A.
·
Bydder G.
·
Sewry C.A.
·
Müller C.
·
Muntoni F.
Document Type
Article
Year published
2005
Published
in Neurology, ISSN: 00283878
Volume: 65, Issue: 12, Pages: 1930-1935 (5)
Indexing
Scopus®
Crossref®117
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 16380615
Scopus: 2-s2.0-33645743730
Source Identifiers
ISSN: 00283878
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