Bestrophin 1 – Phenotypes and Functional Aspects in Bestrophinopathies
Author:
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/13816810.2013.863945
Reference141 articles.
1. Hereditary macular degeneration (HMD) in 246 cases traced to one gene-source in central Sweden
2. The gene for Best's macular dystrophy is located at 11q13 in a Swedish family
3. Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13
4. Identification of the gene responsible for Best macular dystrophy
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2. RPE und Gentherapie;Das Retinale Pigmentepithel – Physiologie und Pathologie;2024
3. Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1);Ophthalmic Genetics;2021-12-13
4. Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies;Acta Ophthalmologica;2021-07-29
5. Structure and Function of the Bestrophin family of calcium-activated chloride channels;Channels;2021-01-01
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