Identification of a novel c.94dupA mutation in RHD allele.

doi:10.1111/trf.16173

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

Community

Back to search

Article

Identification of a novel c.94dupA mutation in RHD allele.

Transfusion - 1 Dec 2020

Deng Danfei, Deng Gang, He Yunlei, Yu Yong

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 Exons
Share to Mutation
Share to Rh-Hr Blood-Group System

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed

Identifiers

PMID: 33140446
DOI: 10.1111/trf.16173

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 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 c.94dupA mutation in RHD allele.PMID 33140446Read ↗

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

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

A novel RHD*DAU allele with c.1136C>T (p.Thr379Met) and c.17C>T (p. Pro6Leu).Semantic proximity Read ↗

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

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

Novel RHD allele with c.333C>G change predicted to encode p.Phe111Leu.Semantic proximity Read ↗

Molecular characterization of 13 new RHD alleles.Semantic proximity Read ↗

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

New RHD variant alleles.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 new RHD variant allele is caused by a RHD 662C>G mutation.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 ↗

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