Seckel syndrome exhibits cellular features demonstrating defects in the ATR signalling pathway

Alderton, G. K., Joenje, H., Varon, R., Borglum, A. D., Jeggo, P. A. and O'Driscoll, M. (2004) Seckel syndrome exhibits cellular features demonstrating defects in the ATR signalling pathway. Human Molecular Genetics, 13. pp. 3127-3138. ISSN 1460-2083

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Item Type: Article
Additional Information: GDSC108
Schools and Departments: School of Life Sciences
Depositing User: Gee Wheatley
Date Deposited: 20 Mar 2007
Last Modified: 30 Nov 2012 16:51
URI: http://sro.sussex.ac.uk/id/eprint/995
Google Scholar:98 Citations
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