<p>FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency</p>

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

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Fassone E, Duncan AJ, Taanman JW et al. FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency. F1000Posters 2011, 2:228 (poster)

FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency

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 Rahman¹ Shamima Rahman² Shamima Rahman³

Published 14 Apr 2011

Author Affiliations

¹ Metabolic Unit, Great Ormond Street Hospital, UK
² MRC Centre for Neuromuscular Diseases, National Hospital for Neurology, UK
³ Clinical and Molecular Genetics Unit, UCL Institute of Child Health, UK

Copyright © 2011 Fassone E et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Published 14 Apr 2011

FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency
[version 1; not peer reviewed]

Author Affiliations

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UK Neuromuscular Translational Research Conference 2011

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Competing Interests

No relevant conflicts of interest declared.

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FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency

FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency [version 1; not peer reviewed]

Terms relating to user comments

FOXRED1 mutations are a novel cause of mitochondrial complex I deficiency
[version 1; not peer reviewed]