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

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.

Transfusion - 1 Jun 2021

Yu Lu, He Yunlei, Xu Deyi, Zhang Jiwei, Deng Gang

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 ABO Blood-Group System
Share to Alleles
Share to Asian People
Share to Mutation

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

Share to Pedigree

Source

Identifiers

PMID: 34075591
DOI: 10.1111/trf.16383

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.PMID 34075591Read ↗

c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.Semantic proximity Read ↗

Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel ABO*A1.02 allele with variant c.671T>C.Semantic proximity Read ↗

Identification of a novel A allele with a c.102C > A variation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel A allele with a c.423 C > A mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.Semantic proximity Read ↗

Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel A allele with c.478C>T missense mutation on the ABO*A1.02 background.Semantic proximity Read ↗

Identification of a novel B allele with a c.917 T > C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

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