Voisset, Cécile

Inserm · Génétique, Génomique Fonctionnelle et Biotechnologies

1 paper on CoChatORCID 0000-0001-7505-1927

Most cited papers

Verified
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

Go further with a free account

Verify every reference, keep papers in a library, and ask questions across them.

Sign up - it is free