Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order Amish. [electronic resource]

By: Contributor(s): Producer: 20150720Description: 767-72 p. digitalISSN:
  • 1097-4598
Subject(s): Online resources: In: Muscle & nerve vol. 51
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Publication Type: Case Reports; Journal Article

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