A novel RHD allele caused by the c.1142G>A mutation identified in a serologic Del phenotype in a Chinese Han male donor

Similar Items

• A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual
  by: Hongjuan Lyu, et al.
  Published: (2024)
• Two novel variant allele of the RHD gene detected in two Chinese blood donors with the RHD negative phenotype
  by: Qiuhong Mo, et al.
  Published: (2025)
• Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)
  by: Jue Hou, et al.
  Published: (2026)
• A serologic weak D caused by a novel RHD allele with single nucleotide c. 209G >C variation predicted to encode p. Arg70Pro
  by: Evelyne Heng, et al.
  Published: (2025)
• Identification of a novel RHD*01W allele with c.175G>T on the RHD*weak partial 15 allele background
  by: Xu Zhang, et al.
  Published: (2026)