Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks

Kerzendorfer, C., Whibley, A., Carpenter, G., Outwin, E., Chiang, Shih-Chieh, Turner, G., Schwartz, C, El-Khamisy, S., Raymond, F.Lucy and O'Driscoll, M. (2010) Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks. Human Molecular Genetics, 19 (7). pp. 1324-1334. ISSN 0964-6906

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Item Type: Article
Additional Information: GDSC312
Schools and Departments: School of Life Sciences > Biochemistry
Subjects: Q Science
Depositing User: Gee Wheatley
Date Deposited: 08 Apr 2010
Last Modified: 07 Mar 2017 08:01
URI: http://sro.sussex.ac.uk/id/eprint/2303
Google Scholar:4 Citations

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