A novel c.29‐3C>G variant on the B allele forms the Bel phenotype

Documents similaires

• Identification of a novel c.506A>C variant on the ABO*A1.02 allele in a Chinese individual
  par: Yongkui Kong, et autres
  Publié: (2024)
• A novel variant c.505C>T based on the ABO*B.01 allele associated with a Bel phenotype
  par: Hua Wang, et autres
  Publié: (2024)
• Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)
  par: Jue Hou, et autres
  Publié: (2026)
• Identification of a novel nonsense variant ( c.184C>T ) in ABO*B.01 allele
  par: Xiaoyun Bu, et autres
  Publié: (2026)
• Identification of a novel B allele with c.155+5G>T in the ABO gene associated with Bweak phenotype
  par: Yu Zhang, et autres
  Publié: (2025)