Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)

Documents similaires

• Identification of a novel RHD*01W allele with c.175G>T on the RHD*weak partial 15 allele background
  par: Xu Zhang, et autres
  Publié: (2026)
• A serologic weak D caused by a novel RHD allele with single nucleotide c. 209G >C variation predicted to encode p. Arg70Pro
  par: Evelyne Heng, et autres
  Publié: (2025)
• Identification of a novel RHD*404T allele in a Chinese individual with variant D phenotype
  par: Yuanyuan Luo, et autres
  Publié: (2025)
• Characterization of a novel ABO allele with variant c. 575T >C on an A1 .01.02 background
  par: Hongli Guan, et autres
  Publié: (2025)
• A novel RHD allele combining partial D (c. 455A >C) and weak D (c. 1154G >C) variants
  par: Glenn Ramsey, et autres
  Publié: (2025)