Wen-jiao Luo
Zhejiang University School Of Medicine And Zhejiang Key Laboratory Of Rare Diseases For Precision Medicine And Clinical Translation
Hangzhou, 310009, China
Hangzhou, 310009, China
Last Updated: 09/26/2026
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Found 9 publications
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: August 27, 2024
Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease.
Journal: Frontiers in genetics
Published: March 31, 2022
Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia.
Journal: Cell discovery
Published: October 29, 2021
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia.
Journal: Molecular genetics & genomic medicine
Published: October 22, 2021
Novel bi-allelic HPDL variants cause hereditary spastic paraplegia in a Chinese patient.
Journal: Clinical genetics
Published: June 23, 2021
TMEM151A variants cause paroxysmal kinesigenic dyskinesia.
Journal: Cell discovery
Published: March 10, 2021
A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: February 05, 2021
Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy.
Journal: Molecular genetics & genomic medicine
Published: August 08, 2019
Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia.
Journal: Clinical genetics
Published: November 29, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026