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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

Author(s)

Jungbluth H.

Lillis S.

Zhou H.

Abbs S.

Sewry C.

Swash M.

Muntoni F.

Tipo de Documento

Article

Year published

2009

Publicado

in Neuromuscular Disorders, ISSN: 0960-8966

Volume: 19, Número: 5, Páginas: 344-347 (3)

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Scopus^®

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Pubmed^®

Google Scholar^®

Publication Identifiers

DOI: 10.1016/j.nmd.2009.02.005

Pubmed: 19303294

SCOPUS: 2-s2.0-67349228165

Source Identifiers

ISSN: 0960-8966

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

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

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