WIDESPREAD DISTRIBUTION OF VARIANT FORMS OF CARBONIC ANHYDRASE IN AUSTRALIAN ABORIGINALS
Author:
Affiliation:
1. Department of Human BiologyJohn Curtin School of Medical ResearchCanberra
Publisher
AMPCo
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.1978.tb107826.x
Reference11 articles.
1. The detection and differentiation of the products of the human carbonic anhydrase loci, CAIand CAIIusing fluorogenic substrates
2. Biochemical genetics of carbonic anhydrase;Tashian R. E.;Advances in Human Genetics,1976
3. Human carbonic anhydrases. VII. A new C type isozyme in erythrocytes of American Negroes
4. The distribution of genetic variants of glyoxalase I, esterase D and carbonic anhydrase I and II in Indian populations;Ghosh A. K.;Indian J. phys. Anthrop, hum. Genet,1977
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1. A HIGH FREQUENCY OF INHERITED DEFICIENCY OF COMPLEMENT COMPONENT C4 IN DARWIN ABORIGINES;Australian and New Zealand Journal of Medicine;1987-08
2. ZINC CONTENT OF RED AND WHITE BLOOD CELLS IN ABORIGINAL CHILDREN;Australian and New Zealand Journal of Medicine;1984-10
3. Human Red Cell Carbonic Anhydrase Variants in Australasia;Annals of the New York Academy of Sciences;1984-06
4. A polymorphic variant of human erythrocyte carbonic anhydrase I with a widespread distribution in Australian aborigines, CAIAustralia-9 (8 Asp ? Gly): Purification, properties, amino acid substitution, and possible physiological significance of the variant enzyme;Biochemical Genetics;1982-10
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