Polymorphism of human alpha fucosidase.
- 1 September 1975
- journal article
- Vol. 27 (5), 651-61
Abstract
A common polymorphism of human alpha fucosidase has been detected by the technique of isoelectric focusing on thin layer acrylamide gel. Family studies have shown that the three common phenotypes Fu 1, Fu 2, and Fu 2-1 represent homozygosity or heterozygosity for two autosomal codominat alleles, Fu1 and Fu2. Frequencies of the Fu1 and Fu2 alleles in the New York populations studied were .753 and .247 among whites and .926 and .074 among blacks, respectively.This publication has 8 references indexed in Scilit:
- Electrophoretic forms of human liver α-l-fucosidase and their relationship to fucosidosis (mucopolysaccharidosis F)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- Isozymes of human α-l-fucosidase detectable by starch gel electrophoresisClinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies.1973
- Linkage Analysis Using Somatic Cell HybridsPublished by Springer Nature ,1972
- FucosidosisThe Journal of Pediatrics, 1969
- Caucasian Genes in American NegroesScience, 1969
- MUCOPOLYSACCHARIDOSIS BY ABSENCE OF α-FUCOSIDASEThe Lancet, 1968
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951