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
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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
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