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Base editing of trinucleotide repeats that cause Huntington’s disease and Friedreich’s ataxia reduces somatic repeat expansions in patient cells and in mice

Title:	Base editing of trinucleotide repeats that cause Huntington’s disease and Friedreich’s ataxia reduces somatic repeat expansions in patient cells and in mice
Authors:	Matuszek, Zaneta^{Aff1, Aff2, Aff3}; Arbab, Mandana^{Aff1, Aff2, Aff4, Aff5, Aff17}; Kesavan, Maheswaran^{Aff6, Aff7}; Hsu, Alvin^{Aff1, Aff2}; Roy, Jennie C. L.^{Aff6, Aff18}; Zhao, Jing^Aff8; Yu, Tian^Aff9; Weisburd, Ben^Aff10; Newby, Gregory A.^Aff11; Doherty, Neil J.^Aff6; Wu, Muzhou^Aff6; Shibata, Shota^{Aff4, Aff6}; Cristian, Ana^{Aff1, Aff2}; Tao, Y. Allen^{Aff1, Aff2}; Fearnley, Liam G.^{Aff12, Aff13}; Bahlo, Melanie^{Aff12, Aff13}; Rehm, Heidi L.^{Aff6, Aff10}; Xie, Jun^Aff14; Gao, Guangping^{Aff14, Aff15}; Mouro Pinto, Ricardo^{Aff4, Aff6, Aff10, IDs41588025021728_cor1}; Liu, David R.^{Aff1, Aff2, Aff16, IDs41588025021728_cor2}
Source:	Nature Genetics. 57(6):1437-1451
Database:	Springer Nature Journals