Fanny Fontaine
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Feb 27, 2026
Mitochondrial Dysfunctions in Human Primary Coenzyme Q<sub>10</sub> Deficiencies.Fanny Fontaine, Romain Pénicaud, Stéphane Allouche
|Jun 27, 2025
Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia.Fanny Fontaine, Audrey Labalme, Chloé Laurencin
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