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High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
2010
359 citations
Journal Article
green Open Access
Field-Weighted Citation Impact:
17.54
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency | Researchclopedia
Center for Human Genetics
Candace Guiducci
·
Broad Institute
Damien L. Bruno
·
Royal Children's Hospital
Olga Goldberger
·
Harvard University
Michelle C Redman
·
Broad Institute
Esko Wiltshire
·
University of Otago
Callum Wilson
·
Starship Children's Health
David Altshuler
·
Massachusetts General Hospital
Stacey B. Gabriel
·
Broad Institute
Mark J. Daly
·
Broad Institute
David R. Thorburn
·
University of Melbourne
Vamsi K. Mootha
·
Massachusetts General Hospital