Loss-of-Function Mutations in thePRPS1Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2


Xuezhong Liu,Dongyi Han,Jianzhong Li,Bing Han,Xiaomei Ouyang,Jing Cheng,Xu Li,Zhanguo Jin,Youqin Wang,Maria Bitner-Glindzicz,Xiangyin Kong,Heng Xu,Albena Kantardzhieva,Roland D. Eavey,Christine E. Seidman,Jonathan G. Seidman,Li L. Du,Zheng-Yi Chen, et al.


The American Journal of Human Genetics




8 January 2010

Copyright © 2010, Elsevier

 User ID  
 Enable Auto Login
Forgot Password/User ID?
If you're a copyright.com user, you can login to RightsLink using your copyright.com credentials.
Already a RightsLink user or want to learn more?

Welcome to RightsLink

Elsevier has partnered with Copyright Clearance Center's RightsLink service to offer a variety of options for reusing Elsevier content. Select the "I would like to ..." drop-down menu to view the many reuse options available to you.

I would like to...


To request permission for a type of use not listed, please contact Elsevier Global Rights Department.

Are you the author of this Elsevier journal article?


Copyright © 2014 Copyright Clearance Center, Inc. All Rights Reserved. Privacy statement.
Comments? We would like to hear from you. E-mail us at customercare@copyright.com