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Results 1 - 5 of 5 for Nemaline myopathy 5
  1. Nemaline myopathy 
    ... Testing Registry: Nemaline myopathy 2 Genetic Testing Registry: Nemaline myopathy 5 Genetic Testing Registry: Nemaline myopathy 6 Genetic Testing ... NB, Sandaradura SA, Clarke NF. Recent advances in nemaline myopathy. Curr Opin Neurol. 2013 Oct;26(5):519-26. doi: 10.1097/WCO.0b013e328364d681. Citation ...
    https://medlineplus.gov/genetics/condition/nemaline-myopathy - Genetics
  2. TPM3 gene 
    ... for a small percentage of all cases of nemaline myopathy. More About This Health Condition cytoskeletal tropomyosin TM30 FLJ41118 heat-stable cytoskeletal protein 30 kDa hscp30 TM-5 TM3 TPM3_HUMAN TRK tropomyosin alpha-3 chain ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  3. TPM2 gene 
    ... mutation. Neurology. 2007 Mar 6;68(10):772-5. doi: 10.1212/01.wnl.0000256339.40667.fb. Citation on PubMed 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
  4. Cap myopathy 
    ... molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy. Biochem J. 2012 Feb 15;442(1):231- ...
    https://medlineplus.gov/genetics/condition/cap-myopathy - Genetics
  5. ACTA1 gene 
    ... the ACTA1 gene have been found to cause nemaline myopathy. Nemaline myopathy is the most common muscle disorder associated with ... ability to contract. ACTA1 gene variants that cause nemaline myopathy impair muscle contraction, causing weakness and the other ...
    https://medlineplus.gov/genetics/gene/acta1 - Genetics