Abstract
Summary
Extensive allelic substitutions at the a and b loci in mice reveal that multiple forms of tyrosinase separable by acryl-amide-gel electrophoresis are subject to complex genetic control. Depending upon genic constitution at the a and b loci, a maximum of three electrophoretically separable forms of tyrosinase are demonstrable. Specific alleles at these loci have also been shown to influence tyrosinase activity.
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