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NDUFA10 mutations cause complex I deficiency in a patient wi…
NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease
NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease
Article, Chapter
Authors: S.J.G. Hoefs
Publication: European Journal of Human Genetics, Volume:19, Issue:3, Page(s):-274
Published: 2011
ISSN: 1018-4813
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View Full Text Source:European Journal of Human Genetics,European Journal of Human Genetics,Springer Complete Journals Opens in new Window
Journal:  European Journal of Human Genetics Source:Springer Complete Journals Opens in new Window
Collection:  Springer Complete Journals Opens in new Window
Coverage:
  • 1993-01-01~present; volume:1~present;issue:1~present
View Full Text Source:European Journal of Human Genetics,European Journal of Human Genetics,PubMed Central Opens in new Window
Journal:  European Journal of Human Genetics Source:PubMed Central Opens in new Window
Collection:  PubMed Central Opens in new Window
Coverage:
  • 2009~12 months ago; volume:17~12 months ago
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