POMT2 mutation in a patient with 'MEB-like' phenotype. [electronic resource]

By: Contributor(s): Producer: 20061010Description: 446-8 p. digitalISSN:
  • 0960-8966
Subject(s): Online resources: In: Neuromuscular disorders : NMD vol. 16
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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