The molecular basis for the B(A) allele: an amino acid alteration in the human histoblood group B alpha-(l,3)-galactosyltransferase increases its intrinsic alpha-(l,3)-N-acetylgalactosaminyltransferase activity.

Yu, LCLCYuLee, HLHLLeeChan, YSYSChanLin, MMLin2010-09-022018-07-062010-09-022018-07-061999-08http://ntur.lib.ntu.edu.tw//handle/246246/194712en-USThe molecular basis for the B(A) allele: an amino acid alteration in the human histoblood group B alpha-(l,3)-galactosyltransferase increases its intrinsic alpha-(l,3)-N-acetylgalactosaminyltransferase activity.