Identification of gene mutations in patients with primary periodic paralysis using targeted next-generation sequencing

Author:

Luo Sushan,Xu Minjie,Sun Jian,Qiao Kai,Song Jie,Cai Shuang,Zhu Wenhua,Zhou Lei,Xi Jianying,Lu Jiahong,Ni Xiaohua,Dou Tonghai,Zhao Chongbo

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,General Medicine

Reference27 articles.

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2. Marchant CL, Ellis FR, Halsall PJ, Hopkins PM, Robinson RL. Mutation analysis of two patients with hypokalemic periodic paralysis and suspected malignant hyperthermia. Muscle Nerve. 2004;30(1):114–7.

3. Zhou H, Lillis S, Loy RE, Ghassemi F, Rose MR, Norwood F, et al. NeuromusculDisord. 2010;20(3):166–73.

4. Nigro V, Piluso G. Next generation sequencing (NGS) strategies for the genetic testing of myopathies. ActaMyol. 2012;31(3):196–200.

5. Dai Y, Wei X, Zhao Y, Ren H, Lan Z, Yang Y, et al. A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencing. NeuromusculDisord. 2015;25(8):617–24.

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