新的临床和分子证据将ARSG突变与Usher综合征IV型联系起来

IF 3.3 2区医学 Q2 GENETICS & HEREDITY

Human Mutation Pub Date : 2022-11-01 DOI:10.1002/humu.24496

Virginie G. Peter, Mathieu Quinodoz, Silvia Sadio, Sebastian Held, Márcia Rodrigues, Marta Soares, Ana Berta Sousa, Luisa Coutinho Santos, Markus Damme, Carlo Rivolta

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引用次数: 0

摘要

Human Mutation, 42, 261-271 (2021) https://doi.org/10.1002/humu.24150The正确的图应该在黑色区域的中心显示一个白色区域(表明保留了视力)，这在文章的发表版本中不是这样的，因此从科学的角度来看是不正确的。正确的数字应该如下图所示:图1出版商为错误道歉。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV

查看原文本刊更多论文

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV

Human Mutation, 42, 261–271 (2021) https://doi.org/10.1002/humu.24150

The correct figure should show a white area in the center of the black field (indicating preserved vision), which is not the case in the published version of the article, and it is therefore incorrect from a scientific standpoint. The correct figure should be as follows:

Figure 1

The publisher apologizes for the error.

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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.