A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family

被引:7
|
作者
Li Xun-hua
Song Chun
Chen Su-qin
Zhou Yan
Guo Hui
Zhou Chun-long
Yang Zhi-yun
Liang Yin-xing
Wang Yi-ming
机构
[1] Sun Yat Sen Univ, Dept Neurol, Guangzhou 510089, Peoples R China
[2] Sun Yat Sen Univ, Dept Radiol, Affiliated Hosp 1, Guangzhou 510089, Peoples R China
[3] Harbin Med Coll, Lab Cellular Transplantat, Affiliated Hosp 1, Harbin 150001, Peoples R China
[4] Sun Yat Sen Univ, Zhongshan Med Coll, Dept Med Genet, Guangzhou 510089, Peoples R China
[5] Chinese Natl Human Genome Ctr Shanghai, Shanghai 201203, Peoples R China
[6] Hangzhou Genom Ctr, Hangzhou 310007, Peoples R China
关键词
hereditary spastic paraplegia; SPG3A; atlastin; mutation; Chinese;
D O I
10.1097/00029330-200705010-00018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:834 / 837
页数:4
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