Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Anais, Thouin"'
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63446 (2013)
Leber Hereditary Optic Neuropathy (LHON) is an important cause of inherited mitochondrial blindness among young adults. The majority of patients carry one of three mitochondrial DNA (mtDNA) point mutations: m.3460G>A, m.11778G>A and m.14484T>C, all o
Externí odkaz:
https://doaj.org/article/3f4ad905d9974aec8542e17a78b892d2
Autor:
Angela, Pyle, Rebecca, Brennan, Marzena, Kurzawa-Akanbi, Alison, Yarnall, Anais, Thouin, Brit, Mollenhauer, David, Burn, Patrick F, Chinnery, Gavin, Hudson
Publikováno v:
Annals of neurology. 78(6)
The identification of cell-free circulating mitochondrial DNA (ccf-mtDNA) in early-stage Alzheimer's disease (AD) raised the possibility that the same neurodegenerative effect could be observed in Parkinson's disease (PD). Here, and for the first tim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbad4c31c2a1eb40c5ce4203d441e23b
https://pubmed.ncbi.nlm.nih.gov/26343811
https://pubmed.ncbi.nlm.nih.gov/26343811