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Mutations in NDUFAF3 %25252528C3ORF60%25252529%2525252C enco…
Mutations in NDUFAF3 %25252528C3ORF60%25252529%2525252C encoding an NDUFAF4 %25252528C6ORF66%25252529-interacting complex I assembly protein%2525252C cause fatal neonatal mitochondrial disease.
Mutations in NDUFAF3 %25252528C3ORF60%25252529%2525252C encoding an NDUFAF4 %25252528C6ORF66%25252529-interacting complex I assembly protein%2525252C cause fatal neonatal mitochondrial disease.
Article, Chapter
Authors: A. Saada
Publication: American Journal of Human Genetics, The, Volume:84, Issue:6
Published: Cell Press, 2009
ISSN: 0002-9297
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View Full Text Source:American Journal of Human Genetics, The,American Journal of Human Genetics, The,Elsevier ScienceDirect Journals Opens in new Window
Journal:  American Journal of Human Genetics, The Source:Elsevier ScienceDirect Journals Opens in new Window
Collection:  Elsevier ScienceDirect Journals Opens in new Window
Coverage:
  • 1997-06~present; volume:60~present;issue:6~present
View Full Text Source:American Journal of Human Genetics, The,American Journal of Human Genetics, The,Cell Press Opens in new Window
Journal:  American Journal of Human Genetics, The Source:Cell Press Opens in new Window
Collection:  Cell Press Opens in new Window
Coverage:
  • 1997-06~present; volume:60~present;issue:6~present
View Full Text Source:American Journal of Human Genetics,American Journal of Human Genetics,PubMed Central Opens in new Window
Journal:  American Journal of Human Genetics Source:PubMed Central Opens in new Window
Collection:  PubMed Central Opens in new Window
Coverage:
  • 1949~6 months ago; volume:1~6 months ago
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