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Genotype-Phenotype Study of Patients With Plaquenil -Induced Retinal Toxicity, With Evaluation of the ABCA4 Gene

• Source: Genotype - Phenotype Study of Patients With Plaquenil-induced Retinal ToxicityLevy GD, Munz SJ, Paschal J, Cohen HB, Pince KJ, Peterson T. Incidence of hydroxychloroquine retinopathy in 1,207

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An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene (POLARIS)

• Source: An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ATP Binding Cassette Subfamily A Member 4

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The ABCA4 gene and age-related macular degeneration: innocence or guilt by association.

• Authors : Gorin, MB

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Identification of Two Novel Mutations in ABCA4 Gene in a Patient With Stargardt Disease.

• Authors : Mohebbi, Masoumeh¹; Heidari, Matin²; Heidari, Mansour³

• Source: Acta Medica Iranica. 2023, Vol. 61 Issue 6, p329-333. 5p.

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Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes.

• Authors : Ścieżyńska, Aneta^1,2 (AUTHOR); Łuszczyński, Krzysztof¹ (AUTHOR); Radziszewski, Marcin¹ (AUTHOR)

Subjects: *RETINOIDS; *HAIR follicles; *STEM cells

• Source: International Journal of Molecular Sciences. May2023, Vol. 24 Issue 9, p8275. 15p.

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Identification of Two Novel Mutations in ABCA4 Gene in a Patient With Stargardt Disease

• Authors : Masoumeh Mohebi; Matin Heidari; Mansour Heidari

Subjects: Stargardt syndrome; ATP binding cassette subfamily a member 4 (ABCA4) gene; Retinitis pigmentosa

• Source: Acta Medica Iranica, Vol 61, Iss 6 (2023)

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The ABCA4 gene and age-related macular degeneration: innocence or guilt by association.

• Authors : Gorin, MB

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Analysis of Retinol Binding Protein 4 and ABCA4 Gene Variation in Non-Neovascular Age-Related Macular Degeneration.

• Authors : Chou, Hung-Da^1,2 (AUTHOR); Hwang, Yih-Shiou^1,2 (AUTHOR); Chen, Kuan-Jen^1,2 (AUTHOR)

• Source: Diagnostics (2075-4418). Jul2023, Vol. 13 Issue 14, p2411. 10p.

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A 12-Year-Old Girl with Bilateral Coats Disease and ABCA4 Gene Mutation

• Authors : Ali Osman Saatci; Ziya Ayhan; Aylin Yaman

Subjects: ABCA4 gene; Coats disease; Dexamethasone implant (Ozurdex)

• Source: Case Reports in Ophthalmology, Vol 9, Iss 2, Pp 375-380 (2018)

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Clinical and Genetic Correlations of Inherital Retinal Disease with Mutations in the ABCA4 Gene by Patients of the Russian Population

• Authors : I. V. Zolnikova; V. V. Kadyshev; A. V. Marakhonov

Subjects: stargardt’s disease; retinitis pigmentosa; abca4

• Source: Oftalʹmologiâ, Vol 18, Iss 4, Pp 897-907 (2021)

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