Suppr超能文献

勘误:神经退行性疾病知识门户:通过共享神经退行性疾病基因组资源推动发现。

Erratum: The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources.

作者信息

Dilliott Allison A, Costanzo Maria C, Bandres-Ciga Sara, Blauwendraat Cornelis, Casey Bradford, Hoang Quy, Iwaki Hirotaka, Jang Dongkeun, Kim Jonggeol Jeffrey, Leonard Hampton L, Levine Kristin S, Makarious Mary, Nguyen Trang T, Rouleau Guy A, Singleton Andrew B, Smadbeck Patrick, Solle J, Vitale Dan, Nalls Mike, Flannick Jason, Burtt Noël P, Farhan Sali M K

出版信息

Neurol Genet. 2025 Jun 3;11(3):e200273. doi: 10.1212/NXG.0000000000200273. eCollection 2025 Jun.

Abstract

[This corrects the article DOI: 10.1212/NXG.0000000000200246.].

摘要

[本文更正了文章的数字对象标识符:10.1212/NXG.0000000000200246。]

相似文献

1
2
Erratum: Missing Full Disclosures.
Neurol Genet. 2024 Nov 1;10(6):e200218. doi: 10.1212/NXG.0000000000200218. eCollection 2024 Dec.
4
The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources.
Neurol Genet. 2025 Feb 21;11(2):e200246. doi: 10.1212/NXG.0000000000200246. eCollection 2025 Apr.
5
Erratum: Medicine, Volume 95, Issue 23: Erratum.
Medicine (Baltimore). 2016 Jul 18;95(28):e0916. doi: 10.1097/01.md.0000489580.04709.16. eCollection 2016 Jul.
6
Erratum: Medicine, Volume 95, Issue 24: Erratum.
Medicine (Baltimore). 2016 Aug 7;95(31):e5074. doi: 10.1097/01.md.0000490009.39850.74. eCollection 2016 Aug.
7
Erratum: Quantitative Muscle MRI to Monitor Disease Progression in Hypokalemic Periodic Paralysis.
Neurol Genet. 2025 Mar 17;11(2):e200255. doi: 10.1212/NXG.0000000000200255. eCollection 2025 Apr.
8
Erratum: Heritability of cervical spinal cord structure.
Neurol Genet. 2020 Mar 18;6(2):e419. doi: 10.1212/NXG.0000000000000419. eCollection 2020 Apr.
9
Erratum: Complex Hybrids Detected in a Cohort of 31 Patients With Spinal Muscular Atrophy.
Neurol Genet. 2024 Oct 23;10(6):e200212. doi: 10.1212/NXG.0000000000200212. eCollection 2024 Dec.
10
Erratum: Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar Ataxia.
Neurol Genet. 2023 Mar 3;9(2):e200065. doi: 10.1212/NXG.0000000000200065. eCollection 2023 Apr.

本文引用的文献

1
The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources.
Neurol Genet. 2025 Feb 21;11(2):e200246. doi: 10.1212/NXG.0000000000200246. eCollection 2025 Apr.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验