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Journal Article
Retina (Philadelphia, Pa.), ISSN 0275-004X, 02/2018, Volume 38, Issue 2, pp. 379 - 386
Purpose: To evaluate the electrooculogram (EOG) in a large series of patients with Best disease and autosomal recessive bestrophinopathy. Methods: A... 
retinal dystrophy | autosomal bestrophinopathy | Best-related retinopathy | Best disease | retina | electrooculography | VMD2 GENE | VITELLIFORM MACULAR DYSTROPHY | POTENTIALS | DEGENERATION | FAMILIES | OPHTHALMOLOGY | RETINOPATHY | MUTATIONS | LIGHT-RISE | CELL | ONSET | Index Medicus
Journal Article
Journal Article
Journal Article
Documenta Ophthalmologica, ISSN 0012-4486, 6/2016, Volume 132, Issue 3, pp. 233 - 243
Journal Article
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, ISSN 0275-004X, 01/2019, Volume 39, Issue 1, pp. E4 - E4
Journal Article
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, ISSN 0275-004X, 09/2015, Volume 35, Issue 9, pp. e58 - e58
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 07/2018, Volume 8, Issue 1, pp. 10176 - 12
Bestinopathies are a spectrum of retinal disorders associated with mutations in BEST1 including autosomal recessive bestrophinopathy (ARB) and autosomal... 
PROTEIN | GENE | AUTOSOMAL RECESSIVE BESTROPHINOPATHY | MEMBRANE | MULTIDISCIPLINARY SCIENCES | PHENOTYPE | RETINOPATHY | CHANNELS | VITELLIFORM MACULAR DYSTROPHY | VMD2 | FAMILY | Transcription | Best vitelliform macular dystrophy | Retina | Heredity | Diagnosis | Mutation | Dystrophy | Genotypes
Journal Article
Journal Article
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, ISSN 0275-004X, 09/2015, Volume 35, Issue 9, pp. e57 - e58
Journal Article
Ophthalmology, ISSN 0161-6420, 01/2018, Volume 125, Issue 1, pp. 75 - 88
Purpose To describe clinical findings in patients with acute exudative polymorphous vitelliform maculopathy (AEPVM). Design Retrospective, observational,... 
AUTOSOMAL RECESSIVE BESTROPHINOPATHY | DYSTROPHY | HYPOTHESIS | DISEASE | OPHTHALMOLOGY | CHOROIDAL NEOVASCULARIZATION | CORTICOSTEROIDS | AUTOFLUORESCENCE | Index Medicus
Journal Article
Genes, ISSN 2073-4425, 02/2019, Volume 10, Issue 2, p. 151
To identify Bestrophin 1 (BEST1) causative mutations in six Lebanese patients from three families, of whom four had a presumed clinical diagnosis of autosomal... 
Mutations | Autosomal recessive bestrophinopathy | Sanger sequencing | Single vitelliform lesion | BEST1 | PROTEIN | VMD2 GENE | PHENOTYPE | VITELLIFORM MACULAR DYSTROPHY | single vitelliform lesion | FAMILY | mutations | DISEASE | GENETICS & HEREDITY | autosomal recessive bestrophinopathy | ONSET | Life Sciences | Genetics | Human genetics
Journal Article
Journal Article