Jinliang Li
Beijing, China
Last Updated: 09/26/2026
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Found 8 publications
SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.
Journal: Frontiers in molecular neuroscience
Published: November 05, 2021
ATP1A1 de novo Mutation-Related Disorders: Clinical and Genetic Features.
Journal: Frontiers in pediatrics
Published: January 22, 2021
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Journal: Journal of medical genetics
Published: September 12, 2019
De novo mutations of TUBB2A cause infantile-onset epilepsy and developmental delay.
Journal: Journal of human genetics
Published: September 11, 2019
Germline de novo variants in CSNK2B in Chinese patients with epilepsy.
Journal: Scientific reports
Published: March 31, 2019
De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsy.
Journal: Epilepsy research
Published: January 21, 2019
Mucopolysaccharidosis IIIB and mild skeletal anomalies: coexistence of NAGLU and CYP26B1 missense variations in the same patient in a Chinese family.
Journal: BMC medical genetics
Published: December 12, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026