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

Two novel FUT1 alleles that cause para-Bombay phenotype in a Chinese individual.

Transfusion - 1 Dec 2020

Lin Feng-Qiu, Zhang Kun-Lian, Li Xiao-Feng, Zhang Xu, Liu Ying, Li Jian-Ping

Abstract excerpt

BACKGROUND: Bombay and para-Bombay phenotypes, which arise from gene mutations of α-1,2-fucosyltransferase FUT1, are very rare in Chinese population. A para-Bombay phenotype Chinese individual with two novel FUT1 mutations was reported here. STUDY DESIGN AND METHODS: The peripheral blood and saliva samples of the proband and her family members were collected after informed consent. ABO and H blood group...

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 China

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

Share to Fucosyltransferases

Share to Galactoside 2-alpha-L-fucosyltransferase

Share to Genotype

Source

Identifiers

PMID: 33175455
DOI: 10.1111/trf.16183

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Two novel FUT1 alleles that cause para-Bombay phenotype in a Chinese individual.PMID 33175455Read ↗

Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants.Semantic proximity Read ↗

Identification of two novel FUT1 mutations in people with Bombay phenotype from Iran.Semantic proximity Read ↗

Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual.Semantic proximity Read ↗

A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.Semantic proximity Read ↗

Analysis of the molecular mechanism and pedigree investigation of para-Bombay phenotype caused by combined mutations at position h649 and h768 of FUT1 gene.Semantic proximity Read ↗

[Identification of a novel FUT1 allele in a Chinese individual featuring para-Bombay phenotype].Semantic proximity Read ↗

Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.Semantic proximity Read ↗

Homozygous FUT1 Mutations Causing a Para-Bombay Phenotype: a Pedigree Investigation Report.Semantic proximity Read ↗

The summary of FUT1 and FUT2 genotyping analysis in Chinese para-Bombay individuals including additional nine probands from Guangzhou in China.Semantic proximity Read ↗

Molecular basis for para-Bombay phenotypes in Chinese persons, including a novel nonfunctional FUT1 allele.Semantic proximity Read ↗

Molecular Genetic Analysis of Para-Bombay Phenotype in Chinese: Identification of a Novel FUT1 Allele.Semantic proximity Read ↗

[Molecular genetic analysis of FUT1 and FUT2 gene in para-Bombay Chinese: a novel FUT1 allele is identified].Semantic proximity Read ↗

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