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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504138/
https://www.ncbi.nlm.nih.gov/pubmed/28508341
http://dx.doi.org/10.1007/s11011-017-0026-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504138/
https://www.ncbi.nlm.nih.gov/pubmed/28508341
http://dx.doi.org/10.1007/s11011-017-0026-0

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