Article
[SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
Zhonghua yi xue za zhi - 1 Nov 1997
Tang B, Wang D, Xia J
Abstract excerpt
OBJECTIVE: To assess the frequency of the SCA1, SCA2, MJD/SCA3 CAG trinucleotide repeat expansions ((CAG)n) among individuals diagnosed with hereditary spinocerebellar ataxia (SCA) from Chinese families. METHOD: The SCA1, SCA2, MJD/SCA3 (CAG)n mutation were detected with the polymerose chain reac...
Topics
- Adolescent
- Adult
- Aged
- Ataxin-1
- Ataxin-3
- Ataxins
- China
- Family Health
- Female
- Gene Frequency
- Humans
- Male
- Middle Aged
- Mutation
- Nerve Tissue Proteins
- Nuclear Proteins
- Proteins
- Repressor Proteins
