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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Metab Brain Dis
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Springer US 2017
Gaiak:
Original Article
Sarrera elektronikoa: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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