The 2588G→C Mutation in theABCRGene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification ofABCRMutations in Patients with Stargardt Disease
Alessandra Maugeri,Marc A. van Driel,Dorien J.R. van de Pol,B. Jeroen Klevering,Frank J.J. van Haren,Nel Tijmes,Arthur A.B. Bergen,Klaus Rohrschneider,Anita Blankenagel,Alfred J.L.G. Pinckers,Niklas Dahl,Han G. Brunner,August F. Deutman, et al.
The American Journal of Human Genetics
Copyright © 1999, Elsevier
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?
Clearance Center, Inc. All Rights Reserved.
Comments? We would like to hear from you. E-mail us at