Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

A Oldfors, H Tajsharghi, L E Thornell

Journal: Neurology 2005;64(3):580-1; author reply 580-1

PMID: 15699411

Full Text on Atypon View on PubMed

Abstract

DOI: 10.1212/wnl.64.3.580-a

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https://www.neurology.org/doi/10.1212/wnl.64.3.580...
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MeSH Terms: Amino Acid Sequence, Amino Acid Substitution, Humans, Hyalin, Inclusion Bodies, Muscular Diseases, Mutation, Missense, Myosin Heavy Chains, Point Mutation, Protein Structure, Tertiary, Sarcolemma

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