[Mitochondrial ATP synthase deficiency due to 8993T > G mutation on ATP6 gene]. [electronic resource]

By: Contributor(s): Producer: 20120419Description: 557-8 p. digitalISSN:
  • 0578-1310
Subject(s): In: Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 49
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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