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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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Publicado no: | Metab Brain Dis |
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Main Authors: | , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Springer US
2017
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Assuntos: | |
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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