Canine MPV17 truncation without clinical manifestations

Mitochondrial DNA depletion syndromes (MDS) are often serious autosomal recessively inherited disorders characterized by tissue-specific mtDNA copy number reduction. Many genes, including MPV17, are associated with the hepatocerebral form of MDS. MPV17 encodes for a mitochondrial inner membrane prot...

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Dettagli Bibliografici
Pubblicato in:Biol Open
Autori principali: Hänninen, Reetta L., Ahonen, Saija, Màrquez, Merce, Myöhänen, Maarit J., Hytönen, Marjo K., Lohi, Hannes
Natura: Artigo
Lingua:Inglês
Pubblicazione: The Company of Biologists 2015
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4610228/
https://ncbi.nlm.nih.gov/pubmed/26353863
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/bio.013870
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