Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients. [electronic resource]

By: Contributor(s): Producer: 19930924Description: 314-20 p. digitalISSN:
  • 1061-4036
Subject(s): Online resources: In: Nature genetics vol. 4
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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