WorldCat Link Resolver, the OpenURL link-server from OCLC

Mutations in NDUFAF3 %252528C3ORF60%252529%25252C encoding a…

Mutations in NDUFAF3 %252528C3ORF60%252529%25252C encoding an NDUFAF4 %252528C6ORF66%252529-interacting complex I assembly protein%25252C cause fatal neonatal mitochondrial disease.

Article, Chapter

Authors: A. Saada

Publication: American Journal of Human Genetics, The, Volume:84, Issue:6, Page(s):718-727

Published: Cell Press

ISSN: 0002-9297

Full text availability for this item

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

Browse related articles

Print copies at your library

Check availability in RUQuest

Request a copy of this item

Cite this item