delta-Aminolevulinate dehydrase: a new genetic polymorphism in man.
作者： G. BATTISTUZZI , R. PETRUCCI , L. SILVAGNI , F. R. URBANI , S. CAIOLA
DOI: 10.1111/J.1469-1809.1981.TB00333.X
关键词:
摘要: SUMMARY A method has been developed for the electrophoretic and quantitative analyses of human red cell δ-aminolevulinate dehydrase (ALADH). The enzyme is under control an autosomal gene, with two common codominant alleles, ALADH1 ALADH2, frequencies 0–89 Oil, respectively, in Italian population. Mean phenotypic activities are nearly identical: 52, 49 55 mlU/g Hb ALADH 1, 2-1 2 phenotypes respectively.
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