Xiaole Wang
87 Xiangya Road
Changsha, China
Changsha, China
Last Updated: 09/26/2026
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Found 8 publications
Heterozygous gain-of-function and mixed-type Kcna2 variants recapitulate SUDEP and increased cortical Npy-Npy1r signaling.
Journal: Neurobiology of disease
Published: April 01, 2026
Biallelic FOXRED1 mutations cause infantile mitochondrial encephalopathy with complex I disassembly and basal ganglia degeneration.
Journal: Mitochondrion
Published: July 27, 2025
Gene therapy with covalently closed-end AAV vector for spinal muscular atrophy.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: April 02, 2025
The genetic spectrum features of 2261 Chinese children with epilepsy and intellectual disability.
Journal: BMC medicine
Published: December 30, 2024
Adeno-associated virus-mediated gene therapy for rare pediatric neurogenetic diseases: Current status and outlook.
Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
Published: December 04, 2023
Novel HCN1 Mutations Associated With Epilepsy and Impacts on Neuronal Excitability.
Journal: Frontiers in molecular neuroscience
Published: February 06, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026