Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families-Reference-Cited by-同舟云学术

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Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families

Published:2021-03-18 Issue:5 Volume:21 Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

He Jialinzi¹,Tang Haiyun²,Liu Chaorong¹,Tan Langzi¹,Xiao Wenbiao¹,Xiao Bo¹,Long Hongyu¹,Long Lili¹

Affiliation:

1. Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China

2. Department of Radiology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Spectrum of Self-Limited Infantile Epilepsy Syndromes;Journal of Pediatric Epilepsy;2024-09-05

2. Exploring epileptic phenotypes in PRRT2-related disorders: A report of two cases and literature appraisal;Seizure: European Journal of Epilepsy;2024-07

3. Evaluation of iron deposition in the motor CSTC loop of a Chinese family with paroxysmal kinesigenic dyskinesia using quantitative susceptibility mapping;Frontiers in Neurology;2023-07-06

4. Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant;Frontiers in Neurology;2023-05-09

5. Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia;Journal of Neurology;2022-04-15

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