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Short report
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family
- Correspondence to Shiro Ikegawa, Laboratory for Bone and Joint Diseases, Center for Genomic Medicine, 4-6-1 Shirokane-dai, Minato-ku, Tokyo 108-8639, Japan; sikegawa{at}ims.u-tokyo.ac.jp
Citation
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family
Publication history
- Received November 27, 2009
- Revised January 26, 2010
- Accepted February 1, 2010
- First published June 24, 2010.
Online issue publication
April 27, 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.