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 the ABO*cis-AB04 Allele With a Unique Substitution C796A: The First Case in Korea.

Annals of laboratory medicine - 1 Nov 2016

Yoon Jung, Youk Hee Jeong, Chang Jung Hee, Jang Mi Ae, Choi Ji Ho, Nam Myung Hyun, Choi Ji Seon, Lim Chae Seung

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 Asian People
Share to Base Sequence
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Polymerase Chain Reaction

Share to Republic of Korea

Share to Sequence Analysis, DNA

Source

Open in PubMed Open full text

Identifiers

PMID: 27578521
DOI: 10.3343/alm.2016.36.6.620
PMCID: PMC5011121

Genes

ABO

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 the ABO*cis-AB04 Allele With a Unique Substitution C796A: The First Case in Korea.PMID 27578521Read ↗

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 B allele with a c.917 T > C mutation on the ABO*B.01 allele.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 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 c.731T>C mutation 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 B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.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 O allele with c.777C>G on an ABO*O.01.02 background.Semantic proximity Read ↗

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

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