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Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.−14C>T mutation in all patients

Authors

  1. Correspondence to Dr Frank Rauch, Shriners Hospital for Children, 1529 Cedar, Montreal, H3G 1A6 Quebec, Canada; frauch{at}shriners.mcgill.ca
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Citation

Rauch F, Moffatt P, Cheung M, et al
Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.−14C>T mutation in all patients

Publication history

  • Received September 15, 2012
  • Revised October 18, 2012
  • Accepted October 19, 2012
  • First published December 13, 2012.
Online issue publication 
December 13, 2012

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