AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease-Reference-Cited by-同舟云学术

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AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease

Published:2023-10 Issue:7 Volume:1869 Page:166760
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Jacobs Howard T.^ORCID,Szibor Marten^ORCID,Rathkolb Birgit^ORCID,da Silva-Buttkus Patricia^ORCID,Aguilar-Pimentel Juan Antonio^ORCID,Amarie Oana V.^ORCID,Becker Lore^ORCID,Calzada-Wack Julia^ORCID,Dragano Nathalia^ORCID,Garrett Lillian^ORCID,Gerlini Raffaele^ORCID,Hölter Sabine M.^ORCID,Klein-Rodewald Tanja^ORCID,Kraiger Markus^ORCID,Leuchtenberger Stefanie^ORCID,Marschall Susan^ORCID,Östereicher Manuela A.^ORCID,Pfannes Kristina^ORCID,Sanz-Moreno Adrián^ORCID,Seisenberger Claudia^ORCID,Spielmann Nadine^ORCID,Stoeger Claudia^ORCID,Wurst Wolfgang^ORCID,Fuchs Helmut^ORCID,Hrabě de Angelis Martin^ORCID,Gailus-Durner Valérie^ORCID

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference80 articles.

1. Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency;Tiranti;Am. J. Hum. Genet.,1998

2. SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome;Zhu;Nat. Genet.,1998

3. Natural history of Leigh syndrome: a study of disease burden and progression;Lim;Ann. Neurol.,2022

4. Mitochondrial disorders of the OXPHOS system;Fernandez-Vizarra;FEBS Lett.,2021

5. Mitochondrial syndromes revisited;Orsucci;J Clin Med,2021

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