Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy in Japanese Cohort

ISCEV Standard for full-field clinical electroretinography (2015 update)

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Identification of the gene responsible for Best macular dystrophy

Konstantin Petrukhin, Markus J. Koisti, Benjamin Bakall et al. · Nature Genetics · 1998 · 686 citations

Medicine, Genetics, Molecular Genetics +12

Bestrophin, the product of the Best vitelliform macular dystrophy gene ( <i>VMD2</i> ), localizes to the basolateral plasma membrane of the retinal pigment epithelium

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The Association Between Percent Disruption of the Photoreceptor Inner Segment–Outer Segment Junction and Visual Acuity in Diabetic Macular Edema

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Health Professions, Ophthalmology, Vision Science +16

Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans

Rosemary Burgess, I. D. Millar, Bart P. Leroy et al. · The American Journal of Human Genetics · 2008 · 313 citations · Full text

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