Xiang Lin
6PUBLICATIONS
7CO-AUTHORS
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Publications (6)
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|Nov 07, 2025
Lysosomal and mTORC1 signaling dysregulation underpin the pathology of spastic paraplegia type 80.Yiqiang Zhi, Tongtong Zhang, Danping Lu
|Oct 29, 2024
A Homoplasmic MT-TV Mutation Associated with Mitochondrial Inheritance of Hereditary Spastic Paraplegia.Yan Shi, Junhao Xie, Junyi Jiang
|Sep 29, 2024
A pseudo-homozygous missense variant and Alu-mediated exon 5 deletion in FARS2 causing spastic paraplegia 77.Shu-Huai Lin, Jun-Hao Xie, Jun-Yi Jiang
|Aug 30, 2020
Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia.Lu-Lu Lai, Yi-Jun Chen, Yun-Lu Li
|Oct 21, 2019
Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia.Miao Zhao, Yi-Jun Chen, Meng-Wen Wang
|Jul 08, 2018
Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China.En-Lin Dong, Chong Wang, Shuang Wu
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