Autosomal Recessive Bestrophinopathy-Reference-Cited by-同舟云学术

Autosomal Recessive Bestrophinopathy

Published:2013-04 Issue:4 Volume:120 Page:809-820
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Boon Camiel J.F.,van den Born L. Ingeborgh,Visser Linda,Keunen Jan E.E.,Bergen Arthur A.B.,Booij Judith C.,Riemslag Frans C.,Florijn Ralph J.,van Schooneveld Mary J.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference55 articles.

1. The spectrum of ocular phenotypes caused by mutations in the BEST1 gene;Boon;Prog Retin Eye Res,2009

2. Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa;Davidson;Am J Hum Genet,2009

3. Functional roles of bestrophins in ocular epithelia;Marmorstein;Prog Retin Eye Res,2009

4. Molecular physiology of bestrophins: multifunctional membrane proteins linked to Best disease and other retinopathies;Hartzell;Physiol Rev,2008

5. Clinical and genetic heterogeneity in multifocal vitelliform dystrophy;Boon;Arch Ophthalmol,2007

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