Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg–Hirschsprung disease: Phenotypes linked by SOX10 mutation
Version of Record online: 22 NOV 2002
Copyright © 2002 Wiley-Liss, Inc.
Annals of Neurology
Volume 52, Issue 6, pages 836–842, December 2002
How to Cite
Inoue, K., Shilo, K., Boerkoel, C. F., Crowe, C., Sawady, J., Lupski, J. R. and Agamanolis, D. P. (2002), Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg–Hirschsprung disease: Phenotypes linked by SOX10 mutation. Ann Neurol., 52: 836–842. doi: 10.1002/ana.10404
- Issue online: 22 NOV 2002
- Version of Record online: 22 NOV 2002
- Manuscript Revised: 13 AUG 2002
- Manuscript Accepted: 13 AUG 2002
- Manuscript Received: 9 APR 2002
- National Institute of Neurological Disorders and Stroke, NIH. Grant Number: R01 NS27042
- Muscular Dystrophy Association
- National Institute of Diabetes, Digestive, and Kidney Diseases, NIH. Grant Number: K08 DK02738
- Research Development Grant from the Muscular Dystrophy Association
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)
- If you already have a Wiley Online Library or Wiley InterScience user account: login above and proceed to purchase the article.
- 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.