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

Zhonghua Er Ke Za Zhi. 2011 Jul;49(7):557-8.
[Article in Chinese]
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Humans
  • Infant
  • Mitochondrial Proton-Translocating ATPases / deficiency*
  • Mitochondrial Proton-Translocating ATPases / genetics*
  • Mutation*

Substances

  • MT-ATP6 protein, human
  • Mitochondrial Proton-Translocating ATPases