勘误:缺少全面披露。

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY Neurology-Genetics Pub Date : 2024-11-01 eCollection Date: 2024-12-01 DOI:10.1212/NXG.0000000000200218
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引用次数: 0

摘要

[此处更正文章 DOI:10.1212/nxg.0000000000200102。][此处更正文章 DOI:10.1212/nxg.0000000000200085。][此处更正文章 DOI:10.1212/nxg.0000000000200099。][此处更正文章 DOI:10.1212/nxg.0000000000200104。.][此处更正文章 DOI:10.1212/nxg.0000000000200083.][此处更正文章 DOI:10.1212/nxg.0000000000200101.][此处更正文章 DOI:10.1212/nxg.0000000000200111.][此处更正文章 DOI:10.1212/nxg.0000000000200081.]。
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Erratum: Missing Full Disclosures.

[This corrects the article DOI: 10.1212/nxg.0000000000200102.][This corrects the article DOI: 10.1212/nxg.0000000000200085.][This corrects the article DOI: 10.1212/nxg.0000000000200099.][This corrects the article DOI: 10.1212/nxg.0000000000200104.][This corrects the article DOI: 10.1212/nxg.0000000000200083.][This corrects the article DOI: 10.1212/nxg.0000000000200101.][This corrects the article DOI: 10.1212/nxg.0000000000200111.][This corrects the article DOI: 10.1212/nxg.0000000000200081.].

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来源期刊
Neurology-Genetics
Neurology-Genetics Medicine-Neurology (clinical)
CiteScore
6.30
自引率
3.20%
发文量
107
审稿时长
15 weeks
期刊介绍: Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. Original articles in all areas of neurogenetics will be published including rare and common genetic variation, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease-genes, and genetic variations with a putative link to diseases. This will include studies reporting on genetic disease risk and pharmacogenomics. In addition, Neurology: Genetics will publish results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials are welcome, including well-powered studies reporting negative results.
期刊最新文献
TRPM8 Mutations Associated With Persistent Pain After Surgical Injury of Corneal Trigeminal Axons. Clinical and Genetic Analysis of 8 Children With Ornithine Transcarbamylase Deficiency: Two Novel Mutations. Disease Progression of GNE Myopathy and Its Relationship With Genotype: A Retrospective, Observational Study in Chinese Patients. Bilateral Dentate Nuclei Hyperintensities and Response to 4-Aminopyridine in a Patient With Childhood-Onset GAA-FGF14-Related Ataxia. Erratum: Missing Full Disclosures.
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