Mitochondrial Encephalomyopathy in Drosophila

Mitochondrial encephalomyopathies are common and devastating multisystem genetic disorders characterized by neuromuscular dysfunction and tissue degeneration. Point mutations in the human mitochondrial ATP6 gene are known to cause several related mitochondrial disorders: NARP (neuropathy, ataxia, an...

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Dades bibliogràfiques
Publicat a:J Neurosci
Autors principals: Celotto, Alicia M., Frank, Adam C., McGrath, Steven W., Fergestad, Tim, Van Voorhies, Wayne A., Buttle, Karolyn F., Mannella, Carmen A., Palladino, Michael J.
Format: Artigo
Idioma:Inglês
Publicat: Society for Neuroscience 2006
Matèries:
Neurobiology of Disease
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6675365/
https://ncbi.nlm.nih.gov/pubmed/16421301
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4162-05.2006
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