Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family with Autosomal Dominant Mitochondrial Myopathy

Mitochondrial myopathies belong to a larger group of systemic diseases caused by morphological or biochemical abnormalities of mitochondria. Mitochondrial disorders can be caused by mutations in either the mitochondrial or the nuclear genome. Only 5% of all mitochondrial disorders are autosomal domi...

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Bibliografiska uppgifter
I publikationen:Neurogenetics
Huvudupphovsmän: Ajroud-Driss, Senda, Fecto, Faisal, Ajroud, Kaouther, Lalani, Irfan, Calvo, Sarah E., Mootha, Vamsi K., Deng, Han-Xiang, Siddique, Nailah, Tahmoush, Albert J., Heiman-Patterson, Terry D., Siddique, Teepu
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2014
Ämnen:
Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4796476/
https://ncbi.nlm.nih.gov/pubmed/25193783
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-014-0421-1
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