Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy. [electronic resource]

By: Contributor(s): Producer: 20191023Description: 675-679 p. digitalISSN:
  • 1873-2364
Subject(s): Online resources: In: Neuromuscular disorders : NMD vol. 28
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Publication Type: Case Reports; Journal Article

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