Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A)

PURPOSE: To describe the clinical features and genetic analysis of a family with an autosomal dominant cone dystrophy (adCD)

Bibliographic Details
Published in:Molecular vision, Vol. 11 (2005), p. 143-51
Main Author: Jiang, Li
Other Involved Persons: Katz, Bradley J ; Yang, Zhenglin ; Zhao, Yu ; Faulkner, Nathan ; Hu, Jianbin ; Baird, Jennifer ; Baehr, Wolfgang ; Creel, Donnell J ; Zhang, Kang
Format: electronic Article
Item Description:Date Completed 03.11.2005
Date Revised 21.11.2008
published: Electronic
Citation Status MEDLINE
Copyright: From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Physical Description:Online-Ressource
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