Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome
M Gerards, 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*
Research output: Contribution to journal › Article › Academic › peer-review
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