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

IF 3.7 2区医学 Q2 GENETICS & HEREDITY

Human Mutation Pub Date : 2025-09-12 DOI:10.1155/humu/9815325

引用次数: 0

Abstract

S. S. Cornelis, M. Bauwens, L. Haer-Wigman, et al., “Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework,” Human Mutation 2023 (2023): 6815504, https://doi.org/10.1155/2023/6815504.

In the article titled “Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework,” there was an error in Figure 1 artwork and caption. The corrected Figure 1 artwork and caption are shown below:

We apologize for this error.

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《使用改良的ACMG/AMP框架阐明Stargardt病变异致病性的2246个独特ABCA4变异临床变异分类纲要》的更正

S. S. Cornelis， M. Bauwens， L. Haer-Wigman，等，“使用改进的ACMG/AMP框架阐明Stargardt病变异致病性的2246个独特ABCA4变异临床变异分类汇编”，《人类突变》2023 (2023)：6815504, https://doi.org/10.1155/2023/6815504.In，题为“使用改进的ACMG/AMP框架阐明Stargardt病变异致病性的2246个独特ABCA4变异临床变异分类纲要”的文章，在图1的插图和标题中有一个错误。更正后的图1插图和标题如下所示：我们为这个错误道歉。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Human Mutation 医学-遗传学

CiteScore

8.40

自引率

5.10%

发文量

190

审稿时长

2 months

期刊介绍： Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of novel DNA variations and their phenotypic consequences, reports of SNPs demonstrated as valuable for genomic analysis, descriptions of new molecular detection methods, and novel approaches to clinical diagnosis are welcomed. Novel reports of gene organization at the genomic level, reported in the context of mutation investigation, may be considered. The journal provides a unique forum for the exchange of ideas, methods, and applications of interest to molecular, human, and medical geneticists in academic, industrial, and clinical research settings worldwide.