HuGE Literature Finder
Records 1 - 2
| 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
| 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
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