Intermediate-Length GGC Repeat Expansion in NOTCH2NLC Was Identified in Chinese Patients with Amyotrophic Lateral Sclerosis

GGC repeat expansions in the 5’ untranslated region (5’UTR) of the Notch Homolog 2 N-terminal-like C gene (NOTCH2NLC) have been reported to be the genetic cause of neuronal intranuclear inclusion disease (NIID). However, whether they exist in other neurodegenerative disorders remains unclear. To det...

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Detalles Bibliográficos
Autores principales: Wan, Mengxia, He, Ji, Huo, Junyan, Sun, Can, Fu, Yu, Fan, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856391/
https://www.ncbi.nlm.nih.gov/pubmed/36672065
http://dx.doi.org/10.3390/brainsci13010085

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856391/
https://www.ncbi.nlm.nih.gov/pubmed/36672065
http://dx.doi.org/10.3390/brainsci13010085

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