Varaico: Literature-Extracted Genetic Variants

Gene:ABCA4
Variant:p.Y1652*
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ABCA4

NM_000350.3:p.Y1652*

Associated Papers

Association Between Genotype and Phenotype Severity in ABCA4-Associated Retinopathy.

Bianco L et al.

Jama Ophthalmology, 2023

Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework.

Cornelis SS et al.

Human Mutation, 2023

40225145 (PubMed )
Supplement: 6815504.f1.zip › S2_PVS1.xlsx › Nonsense_or_Frameshift

Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.

Karali M et al.

Scientific Reports, 2022

36460718 (PubMed )
Supplement: 41598_2022_24636_MOESM2_ESM.xlsx › Supplementary_Table_S1

Genetic characteristics of 234 Italian patients with macular and cone/cone-rod dystrophy.

Falsini B et al.

Scientific Reports, 2022

35260635 (PubMed )
Supplement: 41598_2022_7618_MOESM1_ESM.pdf

A novel statistical method for interpreting the pathogenicity of rare variants.

Wang J et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021

32884132 (PubMed )
Supplement: NIHMS1630822-supplement-Supplementary_Tables.xlsx › S6_ABCA4_variants

ABCA4 gene screening by next-generation sequencing in a British cohort.

Fujinami K et al.

Investigative Ophthalmology & Visual Science, 2013

Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.

Fujinami K et al.

American Journal of Ophthalmology, 2013

A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations.

Fujinami K et al.

American Journal of Ophthalmology, 2013

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

Stenirri S et al.

Clinical Chemistry, 2004

Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients.

Fumagalli A et al.

Human Genetics, 2001

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."