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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 5, 2024. (Total: 234082Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Paraplegia and CAPN1[original query]
Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia.
Translational neurodegeneration 2019 8 19.
Wei Qiao, Dong Hai-Lin, Pan Li-Ying, Chen Cong-Xin, Yan Yang-Tian, Wang Rou-Min, Li Hong-Fu, Liu Zhi-Jun, Tao Qing-Qing, Wu Zhi-Yi
Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia.
Annals of clinical and translational neurology 2020 8 7 (10): 1862-1869.
Lai Lu-Lu, Chen Yi-Jun, Li Yun-Lu, Lin Xiao-Hong, Wang Meng-Wen, Dong En-Lin, Wang Ning, Chen Wan-Jin, Lin Xia
Mutation analysis of CAPN1 in Chinese populations with spastic paraplegia and related neurodegenerative diseases.
Journal of the neurological sciences 2020 Jan 411 116691.
Xia Zheng-Cai, Liu Zhen-Hua, Zhou Xiao-Xia, Liu Zhen, Wang Jun-Ling, Hu Zheng-Mao, Tan Jie-Qiong, Shen Lu, Jiang Hong, Tang Bei-Sha, Lei Li-Fa
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