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New disease loci
Short report
Mutations in WNT1 are a cause of osteogenesis imperfecta

Authors

  1. Correspondence to Dr Frank Rauch, Genetics Unit, Shriners Hospital for Children, 1529 Cedar Avenue, Montréal, Québec, Canada H3G 1A6; frauch{at}shriners.mcgill.ca
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Citation

Fahiminiya S, Majewski J, Mort J, et al
Mutations in WNT1 are a cause of osteogenesis imperfecta
Journal of Medical Genetics 2013;50:345-348.

Publication history

  • Received January 29, 2013
  • Revised February 5, 2013
  • Accepted February 6, 2013
  • First published February 23, 2013.
Online issue publication 
April 27, 2016

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