Article
In vivo somatic mutations in Werner's syndrome.
Human genetics - 1 Oct 1998
Kyoizumi S, Kusunoki Y, Seyama T, Hatamochi A, Goto M
Abstract excerpt
The frequencies of mutant erythrocytes with loss of heterozygosity at the glycophorin A (GPA) locus and mutant CD4+ T cells lacking surface expression of the T-cell receptor alphabeta (TCR)/CD3 complex were measured by flow cytometry for Japanese Werner's syndrome (WRN) patients. The hemizygous a...
Topics
- Adult
- Age Factors
- Bloom Syndrome
- Erythrocytes
- Female
- Flow Cytometry
- Gene Frequency
- Glycophorins
- Humans
- Loss of Heterozygosity
- Male
- Middle Aged
- Mutation
- Receptor-CD3 Complex, Antigen, T-Cell
- Werner Syndrome
