A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family.
- Author:
Xun-hua LI
1
;
Chun SONG
;
Su-qin CHEN
;
Yan ZHOU
;
Hui GUO
;
Chun-long ZHOU
;
Zhi-yun YANG
;
Yin-xing LIANG
;
Yi-ming WANG
Author Information
1. Department of Neurology, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510089, China.
- Publication Type:Journal Article
- MeSH:
Adolescent;
Adult;
Aged;
Child;
Child, Preschool;
China;
ethnology;
Evoked Potentials, Somatosensory;
Evolution, Molecular;
Female;
Foot Deformities, Congenital;
genetics;
GTP Phosphohydrolases;
genetics;
GTP-Binding Proteins;
Genes, Dominant;
Humans;
Male;
Membrane Proteins;
Middle Aged;
Mutation;
Spastic Paraplegia, Hereditary;
genetics
- From:
Chinese Medical Journal
2007;120(9):834-837
- CountryChina
- Language:English
