Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy

OBJECTIVE: Trinucleotide GGC repeat expansion in the 5’UTR of the NOTCH2NLC gene has been recognized as the pathogenesis of neuronal intranuclear inclusion disease (NIID). Previous studies have described that some NIID patients showed clinical and pathological similarities with multiple system atrop...

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Dettagli Bibliografici
Pubblicato in:Ann Clin Transl Neurol
Autori principali: Fang, Pu, Yu, Yanyan, Yao, Sheng, Chen, Shuyun, Zhu, Min, Chen, Yunqing, Zou, Keji, Wang, Lulu, Wang, Huan, Xin, Ling, Hong, Tao, Hong, Daojun
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2020
Soggetti:
Research Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7187708/
https://ncbi.nlm.nih.gov/pubmed/32250060
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51021
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