Long-read sequencing identified repeat expansions in the 5′UTR of the <i>NOTCH2NLC</i> gene from Chinese patients with neuronal intranuclear inclusion disease

Jianwen Deng(Peking University), Zhaoxia Wang(Hefei University), Muliang Gu(Peking University), Jing Bai(Sun Yat-sen University), Sheng Yao(Chinese PLA General Hospital), Pidong Li(Grandomics (China)), Daojun Hong(Nanchang University), Wei Sun(Peking University), Yanan Su(Grandomics (China)), Yun Yuan(Peking University), Fan Li(Bristol-Myers Squibb (United States)), Jun Zhang(Fudan University Shanghai Cancer Center), Yu Miao(Grandomics (China)), Xuefan Yu(Jilin University), Jian Huang(Zhejiang Chinese Medical University), Yining Huang(Nanjing University of Chinese Medicine), Min Zhu(Nanchang University), Fang Pu(University of Science and Technology of China), Jiaxi Yu(Peking University)
Journal of Medical Genetics
August 14, 2019
Cited by 146


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