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

Download in:

• JSON
• RDF
• N3/Turtle
• N-Triples

View as

• Triples