Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Paraplegia and ALDH18A1[original query] |
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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 Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia. Frontiers in neurology 2021 6 12 627531. Chen Yi-Jun, Zhang Zai-Qiang, Wang Meng-Wen, Qiu Yu-Sen, Yuan Ru-Ying, Dong En-Lin, Zhao Zhe, Zhou Hai-Tao, Wang Ning, Chen Wan-Jin, Lin Xia |
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia. Frontiers in neurology 2023 9 14 1239725. Amokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, Lindsay A Wilson, Jana Vandrovcova, Mary M Reilly, Christopher J Record, Michael Benatar, Gang Wu, Sharika Raga, Jo M Wilmshurst, Kireshnee Naidu, Michael Hanna, Melissa Nel, Jeannine M Heckma |
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- Page last updated:Apr 16, 2024
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