Article
Identification of an uncommon haptoglobin type using DNA and protein analysis.
Human genetics - 1 Oct 1993
Marles S L, McAlpine P J, Zelinski T, Phillips S, Maeda N, Greenberg C R
Abstract excerpt
The inherited variations in haptoglobin phenotypes are attributed to the homozygous and heterozygous combinations of three common autosomal alleles: HP*1F, HP*1S and HP*2. HP*1F and HP*1S encode polypeptides that differ by two amino acids at positions 51 and 53. The formation of HP*2 is postulate...
Topics
- Alleles
- Blood Proteins
- Blotting, Southern
- Corneal Dystrophies, Hereditary
- DNA
- Electrophoresis, Starch Gel
- Female
- Genotype
- Haptoglobins
- Humans
- Male
- Nucleic Acid Hybridization
- Phenotype
