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Hereditary Disorders of Erythrocyte Metabolism.
Abstract
Inherited disorders of erythrocyte metabolism have provided a great deal of information on the pathophysiology of congenital hemolytic anemias, and in the wider area of inherited variations in human metabolic pathways. Indeed, the red cell has been to the human biochemical geneticist whatDrosophilawas to the classical geneticist: an extremely useful tool, easily available, and endowed with an amazing number of inherited variations. The present volume represents the proceedings of a symposium held in February 1967; it serves as a review of selected aspects of the rapidly evolving field of inherited variations of erythrocyte metabolism. The topics covered range from a description of some aspects of acatalasemia in Japan by Takahara, to an erudite discussion of the contributions of hereditary red cell enzymopathies, to human genetics by Motulsky. Most important enzyme defects are covered, and the list of participants reads like aWho's Whoin the field. Editor Beutler
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Citations
Cited by
Lipid peroxidation in erythrocytes
Clemens, M. R., & Waller, H. D. (1987) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(87)90068-5 · Cited by 318
Paroxysmal Nocturnal Hemoglobinuria: Evidence for Monoclonal Origin of Abnormal Red Cells
ONI, S. B., OSUNKOYA, B. O., & LUZZATTO, L. (1970) · Blood · doi:10.1182/blood.v36.2.145.145 · Cited by 275
Metadata
- Authors
- Necheles, T. F.
- Venue
- Archives of Internal Medicine
- Publisher
- American Medical Association (AMA)
- Published
- 1968-10-01
- Volume
- 122
- Issue
- 4
- Pages
- 377
- ISSN
- 0003-9926 (ISSN-L)
- OpenAlex
- W1967970633
- Cited by
- 193
- References
- 0
- FWCI
- 23.54
- Type
- journal article
- Language
- en
- Open access
- closed
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