RHD del28Phe encoded by a novel in frame deletion in Exon 1 resulting in a weak D phenotype. Novel in frame deletion RHD del28Phe
收藏NIAID Data Ecosystem2026-03-11 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJEB30851
下载链接
链接失效反馈官方服务：
资源简介：
During routine RHD typing, a novel allele was identified by Sanger sequencing of exons 1-10 and adjacent intronic regions. Molecular analyses confirmed a del28Phe Background.
创建时间：
2019-03-06
