Literature DB >> 19781397

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

Juan Du1, Lu Shen, Guo-hua Zhao, Yin-guang Wang, Shu-sheng Liao, Chong Chen, Zhi-fan Zhou, Ying-ying Luo, Hong Jiang, Kun Xia, Bei-sha Tang.   

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Year:  2009        PMID： 19781397

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN： 0366-6999            Impact factor:   2.628


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  3 in total

1.  Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia.

Authors:  Tae-Hyoung Kim; Jae-Hyeok Lee; Young-Eun Park; Jin-Hong Shin; Tai-Seung Nam; Hyang-Sook Kim; Ho-Jung Jang; Artem Semenov; Sang Jin Kim; Dae-Seong Kim
Journal:  J Clin Neurol       Date:  2014-07-03       Impact factor: 3.077

2.  BmREEPa Is a Novel Gene that Facilitates BmNPV Entry into Silkworm Cells.

Authors:  Xiao-long Dong; Tai-hang Liu; Wei Wang; Cai-xia Pan; Yun-fei Wu; Guo-yu Du; Peng Chen; Cheng Lu; Min-hui Pan
Journal:  PLoS One       Date:  2015-12-14       Impact factor: 3.240

3.  ETS1 variants confer susceptibility to ankylosing spondylitis in Han Chinese.

Authors:  Shan Shan; Jie Dang; Jiangxia Li; Ze Yang; Hailing Zhao; Qian Xin; Xiaochun Ma; Yongchao Liu; Xianli Bian; Yaoqin Gong; Qiji Liu
Journal:  Arthritis Res Ther       Date:  2014-04-04       Impact factor: 5.156
  3 in total

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