Rare FN1 missense mutations indicate a protective role against Lewy body dementia in APOEε4 homozygous carriers.
作者信息
Reho Paolo, Ray Anindita, Kaivola Karri, Vardarajan Badri N, Wu Haotian, Scholz Sonja W
机构信息
Neurodegenerative Diseases Research Section, National Institute of Neurological Disorders and Stroke, Bethesda, MD, 20892-3707, USA.
Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, USA.
出版信息
Acta Neuropathol. 2025 Aug 29;150(1):22. doi: 10.1007/s00401-025-02925-z.
Abstract
摘要
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本文引用的文献
1
Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer's disease.纤维连接蛋白 1 (FN1) 中的罕见遗传变异可预防阿尔茨海默病中的 APOEε4。
Acta Neuropathol. 2024 Apr 10;147(1):70. doi: 10.1007/s00401-024-02721-1.
2
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.基因组测序分析鉴定出与路易体痴呆相关的新基因座，并深入了解其遗传结构。
Nat Genet. 2021 Mar;53(3):294-303. doi: 10.1038/s41588-021-00785-3. Epub 2021 Feb 15.
3
Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium.路易体痴呆的诊断与管理：DLB联盟第四次共识报告
Neurology. 2017 Jul 4;89(1):88-100. doi: 10.1212/WNL.0000000000004058. Epub 2017 Jun 7.
4
Clinical diagnostic criteria for dementia associated with Parkinson's disease.帕金森病相关痴呆的临床诊断标准。
Mov Disord. 2007 Sep 15;22(12):1689-707; quiz 1837. doi: 10.1002/mds.21507.
5
Lewy body pathology in Alzheimer's disease.阿尔茨海默病中的路易体病理改变。
J Mol Neurosci. 2001 Oct;17(2):225-32. doi: 10.1385/jmn:17:2:225.
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