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Early diagnosis of Werner's syndrome using exome-wide sequencing in a single, atypical patient.
journal contribution
posted on 2023-06-07, 20:37 authored by Eleanor Raffan, Liam A Hurst, Saeed Al Turki, Gillian Carpenter, Carol Scott, Allan Daly, Alison Coffey, Sanjeev Bhaskar, Eleanor Howard, Naz Khan, Helen Kingston, Aarno Palotie, David B Savage, Mark O'DriscollMark O'Driscoll, Claire Smith, Stephen O'Rahilly, Inês Barroso, Robert K SempleNo description supplied
History
Publication status
- Published
Journal
Frontiers in Genomic EndocrinologyExternal DOI
Issue
ArticlVolume
2Department affiliated with
- Sussex Centre for Genome Damage Stability Publications
Notes
This was the first article to be published in the inaugural issue of this journal.Full text available
- No
Peer reviewed?
- Yes
Legacy Posted Date
2012-02-06Usage metrics
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