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. 2015 Jun 22;24(14):4183. doi: 10.1093/hmg/ddv164

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

Elisa Fassone, Andrew J Duncan, Jan-Willem Taanman, Alistair T Pagnamenta, Michael I Sadowski, Tatjana Holand, Waseem Qasim, Paul Rutland, Sarah E Calvo, Vamsi K Mootha, Maria Bitner-Glindzicz, Shamima Rahman
PMCID: PMC4476455  PMID: 26022995

Human Molecular Genetics 2010 19:24; pp. 4837–4847; doi: 10.1093/hmg/ddq414

Some Funding was missed from this paper and should be included as follows:

The work was also funded in part by a grant from the US National Institutes of Health (GM077465) awarded to V.K.M.

The authors apologise for this omission.


Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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