• Chinese medical journal · Sep 2009

    Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.

    • Juan Du, Lu Shen, Guo-hua Zhao, Yin-guang Wang, Shu-sheng Liao, Chong Chen, Zhi-fan Zhou, Ying-ying Luo, Hong Jiang, Kun Xia, and Bei-sha Tang.
    • Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
    • Chin. Med. J. 2009 Sep 5; 122 (17): 206420662064-6.

    no abstract available

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