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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Ann Clin Transl Neurol
मुख्य लेखकों: Fang, Pu, Yu, Yanyan, Yao, Sheng, Chen, Shuyun, Zhu, Min, Chen, Yunqing, Zou, Keji, Wang, Lulu, Wang, Huan, Xin, Ling, Hong, Tao, Hong, Daojun
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: John Wiley and Sons Inc. 2020
विषय:
Research Articles
ऑनलाइन पहुंच: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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