Early diagnosis of Werner's syndrome using exome-wide sequencing in a single, atypical patient.

Raffan, Eleanor, Hurst, Liam A, Al Turki, Saeed, Carpenter, Gillian, Scott, Carol, Daly, Allan, Coffey, Alison, Bhaskar, Sanjeev, Howard, Eleanor, Khan, Naz, Kingston, Helen, Palotie, Aarno, Savage, David B, O'Driscoll, Mark, Smith, Claire, O'Rahilly, Stephen, Barroso, Inês and Semple, Robert K (2011) Early diagnosis of Werner's syndrome using exome-wide sequencing in a single, atypical patient. Frontiers in Genomic Endocrinology, 2 (Articl).

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Item Type: Article
Additional Information: This was the first article to be published in the inaugural issue of this journal.
Schools and Departments: School of Life Sciences > Sussex Centre for Genome Damage and Stability
Depositing User: Gillian Carpenter
Date Deposited: 06 Feb 2012 18:35
Last Modified: 30 Nov 2012 17:00
URI: http://sro.sussex.ac.uk/id/eprint/17255
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