These authors contributed equally to this work
LETTER TO THE EDITOR
Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops
Version of Record online: 14 APR 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 3, pages 293–295, March 2014
How to Cite
Beneteau, C., Thierry, G., Blesson, S., Le Vaillant, C., Picard, V., Béné, M.C., Eveillard, M. and Le Caignec, C. (2014), Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops. Clinical Genetics, 85: 293–295. doi: 10.1111/cge.12147
- Issue online: 27 JAN 2014
- Version of Record online: 14 APR 2013
- Manuscript Accepted: 15 MAR 2013
- Manuscript Revised: 14 MAR 2013
- Manuscript Received: 18 FEB 2013
- University Hospital of Nantes. Grant Number: France
Options for accessing this content:
- If you are a society or association member and require assistance with obtaining online access instructions please contact our Journal Customer Services team.
- If your institution does not currently subscribe to this content, please recommend the title to your librarian.
- Login via other institutional login options http://onlinelibrary.wiley.com/login-options.
- You can purchase online access to this Article for a 24-hour period (price varies by title)
- New Users: Please register, then proceed to purchase the article.
Login via OpenAthens
Search for your institution's name below to login via Shibboleth.
Registered Users please login:
- Access your saved publications, articles and searches
- Manage your email alerts, orders and subscriptions
- Change your contact information, including your password
Please register to:
- Save publications, articles and searches
- Get email alerts
- Get all the benefits mentioned below!
Patients and/or caregivers may access this content for use in relation to their own personal healthcare or that of a family member only. Terms and conditions will apply.