Effect of bestrophin-1 on L-type Ca2+ channel activity depends on the Ca2+ channel beta-subunit

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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

Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)

Andreas Marquardt · Human Molecular Genetics · 1998 · 358 citations · Full text

Medicine, Genetics, Molecular Genetics +17

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

Life Sciences, Genetics, Molecular Genetics +14

The Light Peak of the Electroretinogram Is Dependent on Voltage-gated Calcium Channels and Antagonized by Bestrophin (Best-1)

Lihua Y. Marmorstein, Jiang Wu, Precious J. McLaughlin et al. · The Journal of General Physiology · 2006 · 198 citations · Full text

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