Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome.

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Published in J Med Genet on June 18, 2009

Authors

M Gerards1, W Sluiter, B J C van den Bosch, L E A de Wit, C M H Calis, M Frentzen, H Akbari, K Schoonderwoerd, H R Scholte, R J Jongbloed, A T M Hendrickx, I F M de Coo, H J M Smeets

Author Affiliations

1: Department of Genetics and Cell Biology, Unit Clinical Genomics, Maastricht University, Maastricht, The Netherlands.

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