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    Genetic and structural analyses suggest that a novel SPG3A mutation causes severe phenotypes of hereditary spastic paraplegia

    Hereditary spastic paraplegia (HSP) is a group of neurodegenerative diseases. The genotypes and phenotypes of HSP are extremely heterogenous. SPG3A is one of the identified genes underlying HSP, and codes for a G...

    Suqin Chen, Yan Zhou, Xunhua Li, Labu, Shuang Huang… in Chinese Science Bulletin (2006)