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  • 1-10 ل  83 نتائج ل ""ABCA4 gene""

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Subject : electroretinography
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Academic Journal

Early impairment of the full-field photopic negative response in patients with Stargardt disease and pathogenic variants of the ABCA4 gene.

  • Authors : Abed E; Department of Ophthalmology, Policlinico Gemelli, Università Cattolica del Sacro Cuore, Rome, Italy.; Placidi G

Subjects: Mutation*; ATP-Binding Cassette Transporters/ATP-Binding Cassette Transporters/ATP-Binding Cassette Transporters/*genetics ; DNA/DNA/DNA/*genetics

  • Source: Clinical & experimental ophthalmology [Clin Exp Ophthalmol] 2018 Jul; Vol. 46 (5), pp. 519-530. Date of Electronic Publication: 2017 Dec 28.Publisher: Wiley-Blackwell Pub. Asia Country of Publication: Australia NLM ID: 100896531 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

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

Subjects: stargardt’s disease; retinitis pigmentosa; abca4

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

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Academic Journal

ABCA4 Gene Screening by Next-Generation Sequencing in a British CohortNext-Generation Sequencing of ABCA4 in British

Subjects: Genetics; Prevention; Clinical Research

  • Source: Investigative Ophthalmology & Visual Science. 54(10)

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Academic Journal

Electroretinography as a Biomarker to Monitor the Progression of Stargardt Disease.

  • Authors : Sajovic J; Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.; Meglič A

Subjects: Electroretinography* ; ATP-Binding Cassette Transporters*/ATP-Binding Cassette Transporters*/ATP-Binding Cassette Transporters*/genetics; Humans

  • Source: International journal of molecular sciences [Int J Mol Sci] 2022 Dec 18; Vol. 23 (24). Date of Electronic Publication: 2022 Dec 18.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations

Subjects: 0301 basic medicine; Male; DNA Mutational Analysis

  • Source: Investigative ophthalmologyvisual science. 57(1)

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Association between genotype and phenotype in families with mutations in the ABCA4 gene

Subjects: Adult; Male; genetic structures

  • Source: Molecular Vision

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Evaluation of the common variants of the ABCA4 gene in families with Stargardt disease and autosomal recessive retinitis pigmentosa

Subjects: Adult; Male; Heterozygote

  • Source: International journal of molecular medicine. 21(6)

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The natural history of stargardt disease with specific sequence mutation in the ABCA4 gene

Subjects: Adult; Male; medicine.medical_specialty

  • Source: Investigative ophthalmologyvisual science. 50(12)

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ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosa

Subjects: Adult; Male; Adolescent

  • Source: Investigative ophthalmologyvisual science. 43(9)

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Cloning of the canine ABCA4 gene and evaluation in canine cone-rod dystrophies and progressive retinal atrophies

Subjects: Male; Radiation Hybrid Mapping; Polymorphism, Genetic

  • Source: Molecular vision. 10

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  • 1-10 ل  83 نتائج ل ""ABCA4 gene""