1.14.17.1	A318S	site-directed mutagenesis, the enzyme shows a marginal decrease in homospecific activity	745892	
1.14.17.1	A318S	the mutation does not influence enzyme activity	728562	
1.14.17.1	A348E	retained inside cell in a premature endoplasmic reticulum form, also naturally occuring mutation	715661	
1.14.17.1	C1021T	naturally occuring gene polymorphism, determination of the frequency in combat veterans with or without chronic posttraumatic stress disorder, overview	684300	
1.14.17.1	D100E	retained inside cell in a premature endoplasmic reticulum form, also naturally occuring mutation	715661	
1.14.17.1	D331N	retained inside cell in a premature endoplasmic reticulum form, also naturally occuring mutation	715661	
1.14.17.1	D460N	site-directed mutagenesis, the mutant shows reduced expression levels compared to the wild-type enzyme, the mutant shows reduced expression levels compared to the wild-type enzyme	745892	
1.14.17.1	G482R	the mutation has subsequent effect on the activity of the enzyme as it is present close to the active site	728562	
1.14.17.1	L208F	a natural variant - three phenotypes of enzyme isolated: 4 * L208-homoenzyme, 4 * F208-homoenzyme and 2 * F208, 2 * L208-heteroenzyme, no significant difference in kinetic properties	438634	
1.14.17.1	L317P	site-directed mutagenesis, the mutant shows secretory deficiency and is localized in the endoplasmic reticulum	745892	
1.14.17.1	L317P	the mutation does not influence enzyme activity	728562	
1.14.17.1	additional information	construction of chimera: dopamine-betamonooxygenase signal, residue 1-42 appended to peptidylglycine alpha-hydroxylating monoxygenase, result: the signal/anchor domain of enzyme is responsible for its membrane association and is likely to play a key role in the targeting of enzyme to secretory garnules in chromaffin cells and adrenergic neurons	438638	
1.14.17.1	additional information	correlation of plasma dopamine beta-hydroxylase activity with polymorphisms in DBH gene in Eastern Indian population, genotyping, allele frequencies and effects of haplotypes, overview	686029	
1.14.17.1	additional information	genotypic and haplotypic associations of the DBH gene with plasma dopamine beta-hydroxylase activity in African Americans, genotyping, relationship between DBH polymorphisms and pDbetaH in samples, overview	686516	
1.14.17.1	additional information	LvDBH expression is silenced in thoracic ganglia, haemocytes and hepatopancreas of shrimp by treatment with LvDBH-dsRNA for 3 days, a decrease of DBH contents in haemocytes accompanied by decreased levels of norepinephrine and dopamine in hemolymph are observed	744949	
1.14.17.1	R549C	site-directed mutagenesis, the enzyme shows a marginal decrease in homospecific activity, the mutant shows partial secretory deficiency and is localized in the endoplasmic reticulum	745892	
1.14.17.1	R549C	the mutation causes abnormal oligomerization through non-native disulfide bond formation	728562	
1.14.17.1	W544S	site-directed mutagenesis, the enzyme shows a marginal decrease in homospecific activity, the mutant shows reduced expression levels compared to the wild-type enzyme	745892