The American Journal of Human Genetics
Volume 64, Issue 4, April 1999, Pages 1024-1035
The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease
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ABCR
Founder mutation
STGD
Retina
Retinal dystrophies
Genotype-phenotype correlation
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Copyright © 1999 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.