The Haptoglobin-Gene Deletion Responsible for Anhaptoglobinemia
- 1 February 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (2) , 245-252
- https://doi.org/10.1086/301701
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 30 references indexed in Scilit:
- Structure and Expression of H-type GDP-L-Fucose:β-D-Galactoside 2-α-L-Fucosyltransferase Gene (FUT1)Published by Elsevier ,1997
- Two Missense Mutations of H Type α(1,2)Fucosyltransferase Gene (FUT1)Responsible for Para‐Bombay PhenotypeVox Sanguinis, 1997
- Haptoglobin deficiency detected by DNA analysis.SEIBUTSU BUTSURI KAGAKU, 1991
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Duplication within the haptoglobin Hp2 geneNature, 1984
- Is the HpO Phenomenon in Tropical Populations Really Genetic?Human Heredity, 1980
- Ahaptoglobinemia in Northeastern BrazilHuman Heredity, 1969
- Amino-acid Sequence of Alpha Chains of Human HaptoglobinsNature, 1968
- Atypical Segregation of Haptoglobin Types in ManNature, 1958
- Haptoglobin Types in British, Spanish Basque and Nigerian African PopulationsNature, 1958