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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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Bibliographische Detailangaben
Veröffentlicht in:Ann Clin Transl Neurol
Hauptverfasser: Fang, Pu, Yu, Yanyan, Yao, Sheng, Chen, Shuyun, Zhu, Min, Chen, Yunqing, Zou, Keji, Wang, Lulu, Wang, Huan, Xin, Ling, Hong, Tao, Hong, Daojun
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2020
Schlagworte:
Online Zugang: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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