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XRCC1 Mutation is Associated with PARP1 Hyperactivation and Cerebellar Ataxia

XRCC1 is a molecular scaffold protein that assembles multi-protein complexes involved in DNA single-strand break repair(1,2). Here, we show that biallelic mutations in human XRCC1 are associated with ocular motor apraxia, axonal neuropathy, and progressive cerebellar ataxia. XRCC1-mutant patient cel...

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Библиографические подробности
Опубликовано в: :	Nature
Главные авторы:	Hoch, Nicolas, Hanzlikova, Hana, Rulten, Stuart L., Tétreault, Martine, Koumulainen, Emilia, Ju, Limei, Hornyak, Peter, Zeng, Zhihong, Gittens, William, Rey, Stephanie, Staras, Kevin, Mancini, Grazia M.S., McKinnon, Peter J., Wang, Zhao-Qi, Wagner, Justin, Yoon, Grace, Caldecott, Keith W.
Формат:	Artigo
Язык:	Inglês
Опубликовано:	2016
Предметы:	Article
Online-ссылка:	https://ncbi.nlm.nih.gov/pmc/articles/PMC5218588/ https://ncbi.nlm.nih.gov/pubmed/28002403 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature20790
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XRCC1 Mutation is Associated with PARP1 Hyperactivation and Cerebellar Ataxia

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