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

NM_000148.4(FUT1):c.[229C>T;302C>T] with 2 missense variations in the FUT1 gene associated with a para-Bombay phenotype.

Transfusion - 1 Jan 2022

Chen Qing, Feng Chenchen, Srivastava Kshitij, Liu Taixiang, Flegel Willy A, Li Min

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 Fucosyltransferases
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 34792200
DOI: 10.1111/trf.16743
PMCID: PMC9067356

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

NM_000148.4(FUT1):c.[229C>T;302C>T] with 2 missense variations in the FUT1 gene associated with a para-Bombay phenotype.PMID 34792200Read ↗

Identification of a novel FUT1 allele with a nucleotide deletion (c.500del) responsible for para-Bombay phenotype.Semantic proximity Read ↗

Identification of a novel FUT1 allele with c.325_414dup in a Chinese individual with para-Bombay phenotype.Semantic proximity Read ↗

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

Identification of a novel nonfunctional FUT1 allele with 967delG in a Chinese para-Bombay phenotype individual.Semantic proximity Read ↗

A novel FUT1*932A allele associated with the para-Bombay A phenotype in a Chinese individual.Semantic proximity Read ↗

A Case of Para-Bombay Phenotype Caused by Homozygous Mutation of the FUT1 Gene.Semantic proximity Read ↗

Molecular genetic analysis of para-Bombay phenotype in Chinese persons: a novel FUT1 allele is identified.Semantic proximity Read ↗

A novel FUT1 variant allele was identified in a Chinese Para-Bombay individual.Semantic proximity Read ↗

Molecular genetic analysis for the para-Bombay blood group revealing two novel alleles in the FUT1 gene.Semantic proximity Read ↗

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

Novel mutations, including a novel G659A missense mutation, of the FUT1 gene are responsible for the para-Bombay phenotype.Semantic proximity Read ↗

A novel FUT1*c.889C>T allele associated with the para-Bombay AB phenotype and computational evaluation of the mutation effect.Semantic proximity Read ↗

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