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

No abstract is available for this paper.

• Publication year

  2003

• Venue

  Neuromuscular Disorders

• Publication date

  2003-09-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/S0960-8966(03)00101-9PMID 12921789
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2023cites this paper
• Different mouse models of nemaline myopathy harboring Acta1 mutations display differing abnormalities related to mitochondrial biology.

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