Honglan Yang
Changsha, 410013, China
Last Updated: 09/26/2026
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Found 9 publications
Corrigendum to "Impaired PARP1-dependent DNA repair in MORC2 mutations drives axonal degeneration in Charcot-Marie-Tooth disease subtype 2Z and spinal muscular atrophy-like neuromotor disorders" [Pharmacol. Res. 224 (2026) 108103].
Journal: Pharmacological research
Published: February 13, 2026
Impaired PARP1-dependent DNA repair in MORC2 mutations drives axonal degeneration in Charcot-Marie-Tooth disease subtype 2Z and spinal muscular atrophy-like neuromotor disorders.
Journal: Pharmacological research
Published: August 23, 2025
Genotype-phenotype correlations of AR-CMT2S in a cohort of axonal Charcot-Marie-Tooth patients from Central South China.
Journal: Journal of the peripheral nervous system : JPNS
Published: April 03, 2024
Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease.
Journal: Journal of the peripheral nervous system : JPNS
Published: August 17, 2023
The MORC2 p.S87L mutation reduces proliferation of pluripotent stem cells derived from a patient with the spinal muscular atrophy-like phenotype by inhibiting proliferation-related signaling pathways.
Journal: Neural regeneration research
Published: July 25, 2023
Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot-Marie-Tooth Disease.
Journal: Journal of neurology
Published: June 11, 2023
Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south China.
Journal: European journal of neurology
Published: June 07, 2021
The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
Journal: Brain : a journal of neurology
Published: October 03, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026