A Cytoplasmic Suppressor of a Nuclear Mutation Affecting Mitochondrial Functions in Drosophila

Phenotypes relevant to oxidative phosphorylation (OXPHOS) in eukaryotes are jointly determined by nuclear and mitochondrial DNA (mtDNA). Thus, in humans, the variable clinical presentations of mitochondrial disease patients bearing the same primary mutation, whether in nuclear or mitochondrial DNA,...

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Detalles Bibliográficos
Autores principales: Chen, Shanjun, Oliveira, Marcos T., Sanz, Alberto, Kemppainen, Esko, Fukuoh, Atsushi, Schlicht, Barbara, Kaguni, Laurie S., Jacobs, Howard T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2012
Materias:
Investigations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3454878/
https://www.ncbi.nlm.nih.gov/pubmed/22851652
http://dx.doi.org/10.1534/genetics.112.143719

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3454878/
https://www.ncbi.nlm.nih.gov/pubmed/22851652
http://dx.doi.org/10.1534/genetics.112.143719

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