Article
High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect.
Human mutation - 1 Jan 1998
Polyakov A V, Dzenis I G, Baharev V A, Evgrafov O V
Abstract excerpt
No abstract is available from the source.
Topics
- Alternative Splicing
- DNA
- Deoxyribonucleases, Type II Site-Specific
- Family Health
- Female
- Founder Effect
- Gene Frequency
- Heterozygote
- Homozygote
- Humans
- Introns
- Male
- Mutation
- Pedigree
- Point Mutation
- Russia
- Steroid 21-Hydroxylase
