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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Metab Brain Dis
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer US 2017
Témata:
Original Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky