Article
alpha-Thalassaemia.
Bailliere's clinical haematology - 1 Mar 1993
Higgs D R
Abstract excerpt
The large number of naturally occurring mutants of this well-characterized locus provides an excellent opportunity for elucidating the relationship between its structure and function. Comparisons of what has been learned about the alpha-globin locus with complementary observations on the beta-glo...
Topics
- Base Sequence
- Consensus Sequence
- Gene Expression Regulation
- Globins
- Hemoglobin H
- Hemoglobins, Abnormal
- Humans
- Hydrops Fetalis
- Intellectual Disability
- Molecular Sequence Data
- Multigene Family
- Mutation
- alpha-Thalassemia