Frequency of Heterozygotes for Hereditary Galactosaemia in a Normal Population
- 1 January 1967
- journal article
- research article
- Published by S. Karger AG in Human Heredity
- Vol. 17 (4) , 289-298
- https://doi.org/10.1159/000152075
Abstract
Of 542 normal individuals, 13 had concentrations of galactose-1-phosphate-uridyl transferase within the heterozygous range. In 11 of these persons the supposition of the heterozygous state was confirmed by family investigations. The heterozygote frequency was calculated at 1 : 50 and the frequency of abnormal homozygotes (patients with hereditary galactosemia) as 1:10 000 live births. A number of as yet unclarified genetic problems which might influence this calculation are discussed.This publication has 5 references indexed in Scilit:
- Estimation of Frequency of Occurrence of Galactosemia in the PopulationExperimental Biology and Medicine, 1964
- A study of the genetics of galactosaemiaAnnals of Human Genetics, 1962
- A PROCEDURE FOR DETECTING CARRIERS OF GALACTOSEMIAProceedings of the National Academy of Sciences, 1959
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956
- A COENZYME FOR PHOSPHOGLUCOMUTASE1948