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Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts

Huntington disease (HD) is an inherited neurodegenerative disorder caused by mutations in the huntingtin gene. Involvement of mitochondrial dysfunctions in, and especially influence of the level of mitochondrial DNA (mtDNA) on, development of this disease is unclear. Here, samples of blood from 84 H...

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Detalhes bibliográficos
Publicado no:Metab Brain Dis
Main Authors: Jędrak, Paulina, Krygier, Magdalena, Tońska, Katarzyna, Drozd, Małgorzata, Kaliszewska, Magdalena, Bartnik, Ewa, Sołtan, Witold, Sitek, Emilia J., Stanisławska-Sachadyn, Anna, Limon, Janusz, Sławek, Jarosław, Węgrzyn, Grzegorz, Barańska, Sylwia
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5504138/
https://ncbi.nlm.nih.gov/pubmed/28508341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11011-017-0026-0
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