Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cells. [electronic resource]

By: Contributor(s): Producer: 19961004Description: 178-81 p. digitalISSN:
  • 0022-510X
Subject(s): Online resources: In: Journal of the neurological sciences vol. 136
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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