Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.
- Author:
Juan DU
1
;
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
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Asian Continental Ancestry Group; genetics; Child; Child, Preschool; Female; Humans; Infant; Male; Membrane Transport Proteins; genetics; Middle Aged; Mutation; genetics; Polymerase Chain Reaction; Sequence Analysis, DNA; Spastic Paraplegia, Hereditary; genetics; Young Adult
- From: Chinese Medical Journal 2009;122(17):2064-2066
- CountryChina
- Language:English
