Corrigendum to “Functional Analysis of Complex Structural and Splice-Altering Variants in the ARSB Gene Towards the Personalized Antisense-Based Therapy for Mucopolysaccharidosis Type VI Patients”

IF 3.3 2区医学 Q2 GENETICS & HEREDITY

Human Mutation Pub Date : 2025-05-15 DOI:10.1155/humu/9764070

引用次数: 0

Abstract

I. Bychkov, A. Filatova, G. Baydakova, N. Sikora, E. Garifullina, A. Bykova, V. Tabakov, A. Skretnev, M. Skoblov, E. Zakharova, “Functional Analysis of Complex Structural and Splice-Altering Variants in the ARSB Gene Towards the Personalized Antisense-Based Therapy for Mucopolysaccharidosis Type VI Patients,” Human Mutation, 2025, https://doi.org/10.1155/humu/2250030

Additionally, the disclosure statement incorrectly cites reference 37. The disclosure statement should read

“Some of the results of this work were presented earlier in the form of a preprint [38].”

The authors apologize for these errors.

查看原文本刊更多论文

“对ARSB基因复杂结构和剪接改变变异的功能分析，对粘多糖病VI型患者进行个性化的反义治疗”的更正

I. Bychkov， A. Filatova， G. Baydakova， N. Sikora， E. Garifullina， A. Bykova， V. Tabakov， A. Skretnev， M. Skoblov， E. Zakharova，“ARSB基因复杂结构和剪接改变变异的功能分析对粘多糖病VI型患者的个性化反义治疗”，《人类突变》，2025,https://doi.org/10.1155/humu/2250030Additionally，声明错误引用文献37。公开声明应该这样写：“这项工作的一些结果在之前以预印本的形式呈现。”作者为这些错误道歉。

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.