A Novel Missense Mutation in the Spectrin Beta Nonerythrocytic 2 Gene Likely Associated with Spinocerebellar Ataxia Type 5.
- Author:
Li-Zhi LIU
1
;
Ming REN
2
;
Mao LI
1
;
Yu-Ting REN
1
;
Bo SUN
1
;
Xiao-Sun SUN
1
;
Si-Yu CHEN
1
;
Si-Yuan LI
1
;
Xu-Sheng HUANG
1
Author Information
- Publication Type:Case Reports
- MeSH: Adult; Female; Genetic Predisposition to Disease; Humans; Mutation, Missense; genetics; Spectrin; genetics; Spinocerebellar Ataxias; etiology; genetics; Young Adult
- From: Chinese Medical Journal 2016;129(20):2516-2517
- CountryChina
- Language:English
