Gong-lu H. Liu
Shanghai, 200040, China
Last Updated: 09/26/2026
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Found 19 publications
Genotype-phenotype relationship in a cohort of 131 Chinese patients with myotonic dystrophy type 1.
Journal: BMC neurology
Published: August 28, 2025
Factor analysis of effective platelet-producing ability of fetal liver-derived cells
Journal: Zhonghua nei ke za zhi
Published: June 08, 2022
Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia.
Journal: Cell discovery
Published: October 29, 2021
Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy.
Journal: CNS neuroscience & therapeutics
Published: July 14, 2021
A novel frameshift ACTN2 variant causes a rare adult-onset distal myopathy with multi-minicores.
Journal: CNS neuroscience & therapeutics
Published: March 28, 2021
TMEM151A variants cause paroxysmal kinesigenic dyskinesia.
Journal: Cell discovery
Published: March 10, 2021
Clinical and genetic characteristics of Chinese patients with reducing body myopathy.
Journal: Neuromuscular disorders : NMD
Published: October 27, 2020
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.
Journal: Brain : a journal of neurology
Published: August 21, 2020
Identification and functional characterization of novel GDAP1 variants in Chinese patients with Charcot-Marie-Tooth disease.
Journal: Annals of clinical and translational neurology
Published: July 22, 2020
Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy.
Journal: NPJ genomic medicine
Published: June 23, 2020
Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease.
Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease.
Journal: Clinical genetics
Published: March 26, 2019
Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis.
Journal: Aging and disease
Published: January 02, 2019
Last Updated: 09/26/2026