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Nemaline myopathy 5 [Supplementary Concept]

Date introduced: August 25, 2010

MeSH Unique ID: C538397

Heading Mapped to:

Entry Terms:

  • Amish Nemaline Myopathy
  • Nemaline Myopathy, Amish Type
  • Nemaline myopathy, caused by mutation in the troponin t1 gene

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