Feng Li

PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsy

Zhenwei Liu, Qianlei Zhao, Ying-chun Hu, 2021, Seizure.

Different experiences of two PRRT2-associated self-limited familial infantile epilepsy

Zhenwei Liu, Qianlei Zhao, Shiyu Fang, 2020, Acta Neurologica Belgica.

Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

Y. Liu, Zhenwei Liu, Zhen Wang, 2017, Scientific Reports.

Lamotrigine monotherapy for paroxysmal kinesigenic dyskinesia in children

Ying-chun Hu, Feng Li, Zhongdong Lin, 2016, Seizure.

De Novo Germline Mutations in SEMA5A Associated With Infantile Spasms

Y. Lou, Zhenwei Liu, Junzhao Zhao, 2019, Front. Genet..

Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

Y. Liu, Zhenwei Liu, Zhen Wang, 2017, Scientific Reports.

Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without Hypomagnesemia

Wei Wang, Qianlei Zhao, Feixia Zheng, 2021, Frontiers in Genetics.