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Results 1 - 3 of 3 for Nemaline myopathy 7
  1. ACTA1 gene 
    ... C, Nishino I, Lochmuller H, Laing NG. Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1). Neuromuscul Disord. 2006 Oct;16(9-10):541-7. doi: 10.1016/j.nmd.2006.07.018. ...
    https://medlineplus.gov/genetics/gene/acta1 - Genetics
  2. TPM3 gene 
    ... gene are also associated with a condition called nemaline myopathy. People with nemaline myopathy typically have muscle weakness throughout their body, including ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  3. TPM2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Nemaline myopathy More About This Health Condition At least six ... beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. Neuromuscul Disord. 2002 Feb;12(2):151-8. ...
    https://medlineplus.gov/genetics/gene/tpm2 - Genetics