Corrigendum to FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantileonset mitochondrial encephalopathy [Human Molecular Genetics, 19, 24, (2010) 4837-4847] DOI: 10.1093/hmg/ddq414;FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

Human Molecular Genetics

Volumn 19, Issue 24, 2010, Pages 4837-4847

  Fassone, Elisa ^a,b   Duncan, Andrew J ^a   Taanman, Jan Willem ^c   Pagnamenta, Alistair T ^d   Sadowski, Michael I ^e   Holand, Tatjana ^a   Qasim, Waseem ^a   Rutland, Paul ^a   Calvo, Sarah E ^f   Mootha, Vamsi K ^f   Bitner Glindzicz, Maria ^a   Rahman, Shamima ^a,g,h  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF MILAN   (Italy)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d UNIVERSITY OF OXFORD   (United Kingdom)

^e NATIONAL INSTITUTE FOR MEDICAL RESEARCH   (United Kingdom)

^f BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^g NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^h GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; MESSENGER RNA; PROTEIN FOXRED 1; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); UNCLASSIFIED DRUG;

ARTICLE; BIOINFORMATICS; CASE REPORT; CELLULAR DISTRIBUTION; CHILD; COMPLEX 1 DEFICIENCY; ENCEPHALOMYOPATHY; FIBROBLAST; GENE MAPPING; GENE MUTATION; GENE SILENCING; HOMOZYGOSITY; HUMAN; INFANT; MALE; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL ENCEPHALOPATHY; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD; STEADY STATE;

EID: 78649454768     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddv164     Document Type: Erratum

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