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Article

Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation.

The Biochemical journal - 15 Mar 2015

Hejzlarová Kateřina, Kaplanová Vilma, Nůsková Hana, Kovářová Nikola, Ješina Pavel, Drahota Zdeněk, Mráček Tomáš, Seneca Sara, Houštěk Josef

Abstract excerpt

Mutations in the MT-ATP6 gene are frequent causes of severe mitochondrial disorders. Typically, these are missense mutations, but another type is represented by the 9205delTA microdeletion, which removes the stop codon of the MT-ATP6 gene and affects the cleavage site in the MT-ATP8/MT-ATP6/MT-CO...

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Identifiers

PMID: 25588698
DOI: 10.1042/BJ20141462

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25588698-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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