NOTCH2NLC expanded GGC repeats in patients with cerebral small vessel disease

OBJECTIVE: GGC repeat expansions in the human-specific NOTCH2NLC gene have been reported as the cause of neuronal intranuclear inclusion disease (NIID). Given the clinical overlap of cognitive impairment in NIID and cerebral small vessel disease (CSVD), both diseases have white matter hyperintensity...

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Detalles Bibliográficos
Autores principales: Wang, Yun-chao, Fan, Yu, Yu, Wen-Kai, Shen, Si, Li, Jia-Di, Gao, Yuan, Ji, Yan, Li, Yu-Sheng, Yu, Lu-Lu, Zhao, Zi-Chen, Li, Shan-Shan, Ding, Yao, Shi, Chang-He, Xu, Yu-ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176980/
https://www.ncbi.nlm.nih.gov/pubmed/36207023
http://dx.doi.org/10.1136/svn-2022-001631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176980/
https://www.ncbi.nlm.nih.gov/pubmed/36207023
http://dx.doi.org/10.1136/svn-2022-001631

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