Rulten, Stuart L.

University of Sussex

1 paper on CoChatORCID 0000-0001-6772-9232

Most cited papers

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XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia
Care4Rare Canada Consortium, Hoch, N. C., Hanzlikova, H., Rulten, S. L., Tétreault, M., Komulainen, E., Ju, L., Hornyak, P., Zeng, Z., Gittens, W., et al. (2017) · Nature
DNA Repair MechanismsPARP inhibition in cancer therapy
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