Letter to the Editor
Hyaline fibromatosis syndrome resulting from a new homozygous missense mutation, p.Gly116Val, in ANTXR2
Article first published online: 5 JUN 2013
© 2013 Japanese Dermatological Association
The Journal of Dermatology
Volume 40, Issue 8, pages 677–678, August 2013
How to Cite
Tümer, L., Kasapkara, Çiğdem., Fong, K., Serdaroğlu, A. and McGrath, J. A. (2013), Hyaline fibromatosis syndrome resulting from a new homozygous missense mutation, p.Gly116Val, in ANTXR2. The Journal of Dermatology, 40: 677–678. doi: 10.1111/1346-8138.12182
- Issue published online: 5 AUG 2013
- Article first published online: 5 JUN 2013
Options for accessing this content:
- If you would like institutional access 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.
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.