A de novo dominant mutation in ACTA1 causing congenital nemaline myopathy associated with a milder phenotype: expanding the spectrum of dominant ACTA1 mutations. [electronic resource]

By: Contributor(s): Producer: 20130815Description: 239-42 p. digitalISSN:
  • 1873-2364
Subject(s): Online resources: In: Neuromuscular disorders : NMD vol. 23
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Publication Type: Case Reports; Journal Article

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