Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype.

Transfusion - 1 Jul 2018

Zhang Jingwei, Guo Ming, Tian Li

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Asian People
Share to RHD gene
Share to Genotype

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Share to Mutation, Missense

Share to Phenotype

Share to Rh-Hr Blood-Group System

Source

Identifiers

PMID: 29607511
DOI: 10.1111/trf.14604

Genes

RHD

Variants

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype.PMID 29607511Read ↗

A novel missense mutation (c.221G>C) in RHD gene identified in a Chinese woman.Semantic proximity Read ↗

The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype.Semantic proximity Read ↗

A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual.Semantic proximity Read ↗

An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.Semantic proximity Read ↗

A novel RHD allele, RHD c.56C>G (p.Thr19Arg), with Del phenotype identified in a Chinese family.Semantic proximity Read ↗

A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.Semantic proximity Read ↗

A novel RHD (c.509T>G, p.Met170Arg) allele shows weakened D expression.Semantic proximity Read ↗

Identification of a novel c.94dupA mutation in RHD allele.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

A novel RHD allele caused by c.687_689delAAG variant.Semantic proximity Read ↗

A new RHD variant allele caused by an RHD c.1228-1G>C mutation in a Chinese family.Semantic proximity Read ↗

A novel nucleotide deletion in RHAG allele identified in a Chinese Rhnull individual.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.