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Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.
Umeå University, Faculty of Medicine, Integrative Medical Biology, Anatomy.
2005 (English)In: Neurology, ISSN 1526-632X, Vol. 64, no 3, 580-1; author reply 580 p.Article in journal (Other academic) Published
Place, publisher, year, edition, pages
2005. Vol. 64, no 3, 580-1; author reply 580 p.
Keyword [en]
Amino Acid Sequence, Amino Acid Substitution, Humans, Hyalin/*chemistry, Inclusion Bodies/*chemistry, Muscular Diseases/*genetics/metabolism/pathology, Mutation; Missense, Myosin Heavy Chains/chemistry/*genetics, Point Mutation, Protein Structure; Tertiary, Sarcolemma/ultrastructure
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URN: urn:nbn:se:umu:diva-12686PubMedID: 15699411OAI: oai:DiVA.org:umu-12686DiVA: diva2:152357
Available from: 2007-04-19 Created: 2007-04-19 Last updated: 2011-01-12Bibliographically approved

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