Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Ataxia and CAPN1[original query] |
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| 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 |
| Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain. Neurology. Genetics 2022 12 8 (6): e200038. Baviera-Muñoz Raquel, Carretero-Vilarroig Lidón, Vázquez-Costa Juan Francisco, Morata-Martínez Carlos, Campins-Romeu Marina, Muelas Nuria, Sastre-Bataller Isabel, Martínez-Torres Irene, Pérez-García Julia, Sivera Rafael, Sevilla Teresa, Vilchez Juan J, Jaijo Teresa, Espinós Carmen, Millán Jose M, Bataller Luis, Aller Ele |
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