Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation. [electronic resource]

By: Contributor(s): Producer: 20100305Description: 519-21 p. digitalISSN:
  • 1526-632X
Subject(s): Online resources: In: Neurology vol. 74
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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