Chunmei Wang
Shanghai, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Study on Leigh syndrome caused by SURF1 gene mutations and its mechanisms.
Journal: Frontiers in neurology
Published: January 21, 2026
Genotypic and Phenotypic Characteristics of Pediatric X-Adrenoleukodystrophy in a Chinese Cohort.
Journal: Neuropsychiatric disease and treatment
Published: November 20, 2024
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy.
Journal: Molecular genetics & genomic medicine
Published: August 22, 2022
Segawa syndrome caused by TH gene mutation and its mechanism.
Journal: Frontiers in genetics
Published: July 27, 2022
Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases.
Journal: Frontiers in pediatrics
Published: July 18, 2022
The Study on the Clinical Phenotype and Function of HPRT1 Gene.
Journal: Child neurology open
Published: May 07, 2022
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene.
Journal: Stem cell research
Published: February 13, 2022
Prevalence and clinical characteristics of active epilepsy in southern Han Chinese.
Journal: Seizure
Published: January 14, 2014
Investigation of prevalence, clinical characteristics and management of epilepsy in Yueyang city of China by a door-to-door survey.
Journal: Epilepsy research
Published: February 03, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026