A novel A allele with c.689G>T mutation identified in a Chinese individual

Transfusion. 2018 Sep;58(9):2250-2251. doi: 10.1111/trf.14803. Epub 2018 Aug 24.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ABO Blood-Group System / genetics*
  • Alleles
  • Amino Acid Substitution
  • Asian People / genetics
  • Genotype
  • Hemagglutination Tests
  • Heterozygote
  • Humans
  • Mutation, Missense*
  • N-Acetylgalactosaminyltransferases / genetics*
  • Point Mutation*
  • Sequence Analysis, DNA

Substances

  • ABO Blood-Group System
  • N-Acetylgalactosaminyltransferases
  • UDPgalactosamine-galactose acetylgalactosaminyltransferase