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 allele arising from c.912C>A mutation in the α-1,3-N-acetylgalactosaminyltransferase gene in a Chinese individual.

Transfusion - 1 Feb 2021

Zhang Xu, Li Xiaofeng, Liu Ying, Li Jianping

Abstract excerpt

BACKGROUND: The Am phenotype, which arises from mutations of the α-1,3-N-acetylgalactosaminyltransferase gene, is rare in the Chinese population. The present study focuses on a novel mutation with the Am phenotype in a Chinese individual. STUDY DESIGN AND METHODS: The sample with ABO blood group discrepancy was analyzed by serologic techniques. The full coding and flanking regions of the ABO gene, including the...

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 Aged
Share to Alleles

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Asian People

Share to N-Acetylgalactosaminyltransferases

Share to Point Mutation

Source

Identifiers

PMID: 33098315
DOI: 10.1111/trf.16159

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel allele arising from c.912C>A mutation in the α-1,3-N-acetylgalactosaminyltransferase gene in a Chinese individual.PMID 33098315Read ↗

[Study of 467C>T and 745C>T variants of alpha-1, 3-N-acetylgalactoseaminotransferase gene].Semantic proximity Read ↗

[Variants 467C > T and 539G > C of the alpha-1,3-N-acetylgalactosaminyltransferase allele responsible for A2 subgroup].Semantic proximity Read ↗

[Ael subgroup due to alpha-1,3-N-acetylgalactoseaminotransferase gene 467C>T and 804insG variants].Semantic proximity Read ↗

[Study of a Chinese pedigree carrying a novel variant of α-1, 3-N-acetyl galactosaminyl transferase gene].Semantic proximity Read ↗

α-1,3-N-acetylgalactose aminotransferase gene 539G>C mutation leads to the A2B isoform.Semantic proximity Read ↗

[Molecular mechanism underlying an individual with with Ael subtype due to a novel p.Tyr264Cys variant of α-1, 3-N-acetylgalactosaminotransferase gene].Semantic proximity Read ↗

A novel A allele with 664G>A mutation identified in a family with the Am phenotype.Semantic proximity Read ↗

[A A311 blood group gene subtype caused by a-1-3-N-acetylgalactosaminyltransferase gene exon 7 mutations].Semantic proximity Read ↗

[Identification of a novel T421C mutation of α-1,3-N-acetylgalactosaminyltransferase allele responsible for an A variant].Semantic proximity Read ↗

[Analysis of a Chinese pedigree with Bw subtype due to a novel variant of α-1,3-N-acetylgalactosaminyltransferase gene].Semantic proximity Read ↗

[Study on a 905A to G mutation of α 1,3 galactosyltransferase gene].Semantic proximity Read ↗

Identification of a Novel Mutation in B Allele in a Chinese Individual.Semantic proximity Read ↗

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