- Genetic variations in Bestrophin‑1 and associated clinical findings in two Chinese patients with juvenile‑onset and adult‑onset best vitelliform macular dystrophy
Ying Lin et al, 2017, Molecular Medicine Reports CrossRef - Clinical Genetics of Vitelliform Macular Dystrophy: An Asian Perspective
Sung Wook Park et al, 2019, Advances in Vision Research, Volume II CrossRef - “Novel p.Tyr284Cys BEST1 genotype–phenotype correlations of Vitelliform Macular Dystrophy in a family with incomplete penetrance”
Lucas Antonio Garza-Garza et al, 2020, Ophthalmic Genetics CrossRef - Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma
Tao Li et al, 2017, Molecular Medicine Reports CrossRef - Ion Channels in Neurological Disorders
Pravir Kumar et al, 2016, Ion Channels as Therapeutic Targets, Part A CrossRef - An allosteric mechanism of inactivation in the calcium-dependent chloride channel BEST1
George Vaisey et al, 2018, Journal of General Physiology CrossRef - Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy
Ying Lin et al, 2017, Molecular Medicine Reports CrossRef - A novel mutation of BEST1 gene in Best disease
Claudio Campa et al, 2021, European Journal of Ophthalmology CrossRef - Vitelliform Macular Dystrophy
Min Kim et al, 2022, Inherited Retinal Disease CrossRef