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

MLA

Wei Sun, et al. “Long-Read Sequencing Identified Repeat Expansions in the 5′UTR of the NOTCH2NLC Gene from Chinese Patients with Neuronal Intranuclear Inclusion Disease.” Journal of Medical Genetics, vol. 56, Aug. 2019, pp. 758–64. EBSCOhost, https://doi.org/10.1136/jmedgenet-2019-106268.

APA

Wei Sun, Pu Fang, Jun Zhang, Zhaoxia Wang, Sheng Yao, Muliang Gu, Yun Yuan, Xue-Fan Yu, Min Zhu, Jing Bai, Yanan Su, Yining Huang, Jianwen Deng, Jiaxi Yu, Fan Li, Jian Huang, Pidong Li, Daojun Hong, & Yu Miao. (2019). Long-read sequencing identified repeat expansions in the 5′UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease. Journal of Medical Genetics, 56, 758–764. https://doi.org/10.1136/jmedgenet-2019-106268

Chicago

Wei Sun, Pu Fang, Jun Zhang, Zhaoxia Wang, Sheng Yao, Muliang Gu, Yun Yuan, et al. 2019. “Long-Read Sequencing Identified Repeat Expansions in the 5′UTR of the NOTCH2NLC Gene from Chinese Patients with Neuronal Intranuclear Inclusion Disease.” Journal of Medical Genetics 56 (August): 758–64. doi:10.1136/jmedgenet-2019-106268.