Identification of a novel RHD*01W allele with c.175G>T on the RHD*weak partial 15 allele background

Ähnliche Einträge

• A novel RHD*01N allele harboring a c.634+ 1G >A splice site variant results in the RhD ‐negative phenotype in a Chinese blood donor
  von: Xu Zhang, et al.
  Veröffentlicht: (2025)
• Identification of a novel DEL allele with c.411G>C on the RHD*01EL.01 allele background
  von: Lin‐Nan Shao, et al.
  Veröffentlicht: (2024)
• Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)
  von: Jue Hou, et al.
  Veröffentlicht: (2026)
• A novel RHD allele combining partial D (c. 455A >C) and weak D (c. 1154G >C) variants
  von: Glenn Ramsey, et al.
  Veröffentlicht: (2025)
• A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual
  von: Hongjuan Lyu, et al.
  Veröffentlicht: (2024)