Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/5200796.pdf
Reference7 articles.
1. Sonnhammer EL, Durbin R . Analysis of protein domain families in Caenorhabditis elegans Genomics 1997 46: 200–216
2. Marquardt A, Stöhr H, Passmore LA et al. Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease) Hum Mol Gen 1998 7: 1517–1525
3. Petrukhin K, Koisti MJ, Bakall B et al. Identification of the gene responsible for Best macular dystrophy Nat Genet 1998 19: 241–247
4. Marmorstein AD, Marmorstein LY, Rayborn M et al. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localises to the basolateral plasma membrane of the retinal pigment epithelium Proc Natl Acad Sci USA 2000 97: 12758–12763
5. . VMD2 Mutation Database at http://www.uni-wuerzburg.de/humangenetics/vmd2.html
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