Article info
Original article
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population
- Correspondence to Dr Elise Héon, Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, 555 University Avenue, Room M165, Toronto, Ontario M5G 1X8, Canada; eheon{at}attglobal.net
Citation
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population
Publication history
- Received September 11, 2009
- Revised January 12, 2010
- Accepted January 27, 2010
- First published May 14, 2010.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.