BEST Disease and Gene Therapy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology
Reference36 articles.
1. Identification of the gene responsible for Best macular dystrophy;Petrukhin;Nat Genet,1998
2. Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best’s disease);Marquardt;Hum Mol Genet,1998
3. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the RPE;Marmorstein;Proc Natl Acad Sci USA,2000
4. The vitelliform macular dystrophy protein defines a new family of chloride channels;Sun;Proc Natl Acad Sci USA,2002
5. iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration;Singh;Hum Mol Genet,2013
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