Loaëc, Nadège

Inserm · Génétique, Génomique Fonctionnelle et Biotechnologies

1 paper on CoChatORCID 0000-0001-5567-0210

Most cited papers

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A homozygous splice variant in ATP5PO , disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families
Ganapathi, M., Friocourt, G., Gueguen, N., Friederich, M. W., Le Gac, G., Okur, V., Loaëc, N., Ludwig, T., Ka, C., Tanji, K., et al. (2022) · Journal of Inherited Metabolic Disease
Mitochondrial Function and PathologyMetabolism and Genetic Disorders
Cited by 18

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