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Article

Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1)

13 Feb 2015

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 25747004
DOI: 10.1016/j.nmd.2015.02.003

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Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1)PMID 25747004Read ↗

Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1).Semantic proximity Read ↗

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An Update on Reported Variants in the Skeletal Muscle α‐Actin (ACTA1) GeneSemantic proximity Read ↗

Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).Semantic proximity Read ↗

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Congenital myopathies: diseases of the actin cytoskeleton.Semantic proximity Read ↗

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Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.Semantic proximity Read ↗

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Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.Semantic proximity Read ↗

Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin gene.Semantic proximity Read ↗

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