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Results 1 - 3 of 3 for Congenital nemaline myopathy
  1. ACTA1 gene 
    ... magnetic resonance imaging and histopathology in ACTA1-related congenital nemaline myopathy. Muscle Nerve. 2014 Dec;50(6):1011-6. doi: 10.1002/mus.24353. Epub 2014 Oct 30. Citation on PubMed ... of ACTA1-related congenital fiber type disproportion. Ann Neurol. 2007 Jun;61( ...
    https://medlineplus.gov/genetics/gene/acta1 - Genetics
  2. TPM2 gene 
    ... Tajsharghi H, Ohlsson M, Lindberg C, Oldfors A. Congenital myopathy with nemaline rods and cap structures caused by a mutation ...
    https://medlineplus.gov/genetics/gene/tpm2 - Genetics
  3. TPM3 gene 
    ... contraction leads to muscle weakness in people with congenital fiber-type disproportion. More About This Health Condition Mutations in the TPM3 gene are also associated with a condition called nemaline myopathy. People with nemaline myopathy typically have muscle weakness ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics