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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Detaylı Bibliyografya
Yayımlandı:Ann Clin Transl Neurol
Asıl Yazarlar: Fang, Pu, Yu, Yanyan, Yao, Sheng, Chen, Shuyun, Zhu, Min, Chen, Yunqing, Zou, Keji, Wang, Lulu, Wang, Huan, Xin, Ling, Hong, Tao, Hong, Daojun
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2020
Konular:
Research Articles
Online Erişim: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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