Identification of telomere dysfunction in Friedreich ataxia

BACKGROUND: Friedreich ataxia (FRDA) is a progressive inherited neurodegenerative disorder caused by mutation of the FXN gene, resulting in decreased frataxin expression, mitochondrial dysfunction and oxidative stress. A recent study has identified shorter telomeres in FRDA patient leukocytes as a p...

詳細記述

保存先:
書誌詳細
出版年:Mol Neurodegener
主要な著者: Anjomani Virmouni, Sara, Al-Mahdawi, Sahar, Sandi, Chiranjeevi, Yasaei, Hemad, Giunti, Paola, Slijepcevic, Predrag, Pook, Mark A.
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2015
主題:
Research Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4462004/
https://ncbi.nlm.nih.gov/pubmed/26059974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13024-015-0019-6
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料