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Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population
  1. 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
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Billingsley G, Bin J, Fieggen KJ, et al
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 
June 30, 2010

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