Answers are grounded in this paper and cite their sources.
Two adults with beta-galactosidase deficiency were studied. Differences in a number of beta-galactosidase parameters (pH optima, heat denaturation, NaCl kinetics) were noted between the patients. Differences were also noted in beta-galactosidase electrophoretic mobilities and urinary oligosaccharides; however, there was no complementation in cell fusion studies. It is suggested that these two patients have different primary mutations at the beta-galactosidase locus which are probably structural in nature.
No takes yet. Share an insight, caveat, or question.
Taylor et al. (1980) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: