Associated Papers
Phenotypic description and functional characterization of the mitochondrial disease associated with the SFXN4 gene.
Courtois S et al.
Mitochondrion, 2026
Primary mitochondrial disorders and mimics: Insights from a large French cohort.
Rouzier C et al.
Annals of Clinical and Translational Neurology, 2024
38703036 (PubMed )
Supplement: ACN3-11-1478-s004.xlsx › children_patients
Hereditary myopathies associated with hematological abnormalities.
Beecher G et al.
Muscle & Nerve, 2022
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4.
Hildick-Smith GJ et al.
American Journal of Human Genetics, 2013
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