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Article

A serologic weakly reactive RhD is caused by a c.496C>G (p.His166Asp) in RHD gene.

Transfusion - 1 Nov 2016

Zhao Hong, Tian Li, Chen Jian

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27611600
DOI: 10.1111/trf.13776

Genes

RHD

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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A serologic weakly reactive RhD is caused by a c.496C>G (p.His166Asp) in RHD gene.PMID 27611600Read ↗

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A novel RHD allele, with c.491A > T (p.Asp164Val) mutation, identified via family pedigree analysis.Semantic proximity Read ↗

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.Semantic proximity Read ↗

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