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

Alderton, Gemma K, Joenje, Hans, Varon, Raymonda, Børglum, Anders D, Jeggo, Penny A and O'Driscoll, Mark (2004) Seckel syndrome exhibits cellular features demonstrating defects in the ATR signalling pathway. Human Molecular Genetics, 13(24). pp. 3127-3138. ISSN 0964-6906

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Item Type: Article
Schools and Departments: School of Life Sciences > Sussex Centre for Genome Damage and Stability
Depositing User: Penny Jeggo
Date Deposited: 06 Feb 2012 19:39
Last Modified: 30 Mar 2012 10:58
URI: http://sro.sussex.ac.uk/id/eprint/21652
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