Catalase Abnormality in a Caucasian Family in the United States
- 17 May 1963
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 140 (3568) , 816-817
- https://doi.org/10.1126/science.140.3568.816
Abstract
An erythrocyte catalase with atypical electromigration velocity was discovered in three generations of a family of Scandinavian-British extraction. Six members are heterozygous for the hereditary autosomal character; no abnormal homozygotes were found. The condition is associated with normal erythrocyte catalase activity and with no clinical or subclinical disease.Keywords
This publication has 4 references indexed in Scilit:
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- Alkaline Phosphatase in Human Sera and PlacentaeScience, 1961
- HYPOCATALASEMIA: A NEW GENETIC CARRIER STATE*Journal of Clinical Investigation, 1960
- Carrier State in Human AcatalasemiaScience, 1959