The molecular basis for the B(A) allele: An amino acid alteration in the human histoblood group B α-(1,3)-galactosyltransferase increases its intrinsic α-(1,3)-N-acetylgalactosaminyltransferase activity

LUNG-CHIH YULee, Hui-LinHui-LinLeeChan, Yung-SyuYung-SyuChanLin, MarieMarieLin2020-01-222020-01-2219990006291Xhttps://scholars.lib.ntu.edu.tw/handle/123456789/452671https://www2.scopus.com/inward/record.uri?eid=2-s2.0-0033609969&doi=10.1006%2fbbrc.1999.1246&partnerID=40&md5=45d48e15e83716a07aad79b1a3f161beThe molecular basis for the B(A) allele: An amino acid alteration in the human histoblood group B α-(1,3)-galactosyltransferase increases its intrinsic α-(1,3)-N-acetylgalactosaminyltransferase activityjournal article10.1006/bbrc.1999.1246104625012-s2.0-0033609969