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Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase
scientific article published on 17 December 2013
Author/s
author: Christine Bôle-Feysot, Patrick Nitschké, Agnès Delahodde, Pascale de Lonlay, Dominique Chrétien, Nathalie Boddaert
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Publication date
December 17, 2013
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