Article info
PDFGenotype-phenotype correlations
Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.−14C>T mutation in all patients
- Correspondence to Dr Frank Rauch, Shriners Hospital for Children, 1529 Cedar, Montreal, H3G 1A6 Quebec, Canada; frauch{at}shriners.mcgill.ca
Citation
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
January 13, 2017
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