Associated Papers
Connecting the Dots: Mitochondrial Dysfunction, PCOS, and Insulin Resistance-Insights and Therapeutic Advances.
Tharayil SP et al.
International Journal of Molecular Sciences, 2025
[Molecular bases of diseases caused by mutations in genes encoding subunits of ATP synthase].
Baranowska E et al.
Postepy Biochemii, 2018
Application of High-Throughput Sequencing in the Diagnosis of Inherited Thrombocytopenia.
Wang Q et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2018
Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease.
Saada A et al.
American Journal of Human Genetics, 2009
Disease-related mutations in cytochrome c oxidase studied in yeast and bacterial models.
Bratton M et al.
European Journal of Biochemistry, 2003
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