更正 "CLCN6 基因突变是患者和小鼠模型中神经元类色素沉着病的新遗传病因"。

IF 8.1 1区医学 Q1 CLINICAL NEUROLOGY

Annals of Neurology Pub Date : 2024-08-29 DOI:10.1002/ana.27076

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引用次数: 0

摘要

He, H, Cao, X, He, F, et al.CLCN6基因突变是患者和小鼠模型神经细胞类脂膜炎的新型遗传病因Ann Neurol 2024; 96: 608-624. https://doi.org/10.1002/ana.27002 在上述文章中，标题被错误地发布为 "Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in a Murine Model"。正确的标题是 "Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model"。本文的在线版本已作相应更正。我们对此错误深表歉意。

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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Correction to “Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model”

He, H, Cao, X, He, F, et al. Mutations in CLCN6 as a novel genetic cause of neuronal ceroid lipofuscinosis in patients and a murine model. Ann Neurol 2024; 96: 608–624. https://doi.org/10.1002/ana.27002

In the above article, the title was incorrectly published as “Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in a Murine Model.”

The correct title is “Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model.” The online version of this article has been corrected accordingly.

We apologize for this error.

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来源期刊

Annals of Neurology 医学-临床神经学

CiteScore

18.00

自引率

1.80%

发文量

270

审稿时长

3-8 weeks

期刊介绍： Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.