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Science 29 July 1977:
Vol. 197. no. 4302, pp. 471 - 472
DOI: 10.1126/science.406674
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Articles

Science, Vol 197, Issue 4302, 471-472
Copyright © 1977 by American Association for the Advancement of Science

articles

Erythrocyte carbonic anhydrase I: inherited deficiency in humans

AG Kendall and RE Tashian

The virtually complete absence of erythrocyte carbonic anhydrase I is reported in three members of a family from the Greek island of Icaria. Two members with moderately reduced levels are believed to be heterozygous for the deficiency. There are no obvious hematological or renal consequences of the severe deficiency state.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Carbonic Anhydrase II Binds to the Carboxyl Terminus of Human Band 3, the Erythrocyte Cl-/HCO3- Exchanger.
J. W. Vince and R. A. F. Reithmeier (1998)
J. Biol. Chem. 273, 28430-28437
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