首页|期刊导航|中华医学杂志(英文版)|A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family
中华医学杂志(英文版)2007,Vol.120Issue(9):834-837,4.
A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family
A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family
摘要
关键词
hereditary spastic paraplegia/SPG3A/atlastin/mutation/ChineseKey words
hereditary spastic paraplegia/SPG3A/atlastin/mutation/Chinese分类
医药卫生引用本文复制引用
LI Xun-hua,SONG Chun,CHEN Su-qin,ZHOU Yan,GUO Hui,ZHOU Chun-long,YANG Zhi-yun,LIANG Yin-xing,WANG Yi-ming..A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family[J].中华医学杂志(英文版),2007,120(9):834-837,4.基金项目
This study was supported by the grants from the Chinese 863 HiTech Project (No.2001AA221102), the Guangdong Provincial Natural Science Foundation (No.031673), the Guangzhou Municipal Science and Technology Bureau (No. 2002Z3-C7191 and No.2004Z3-C7501),the PhD Station of Higher Education Fund of the Ministry of Education (No.2004-18) and the China Medical Boarl of New York (No.01-795). (No.2001AA221102)