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 GYPA*01 allele with a c.125C > G (p.Thr42Ser) mutation identified in a Chinese individual.

Transfusion - 1 May 2021

Liang Yan-Lian, Liang Shuang, Tang Xiong-Chi, Su Yu-Qing, Wu Fan, Peng Long, Xu Yun-Ping

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 Alleles
Share to Asian People
Share to China
Share to Erythrocytes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glycophorins

Share to Point Mutation

Source

Identifiers

PMID: 33682118
DOI: 10.1111/trf.16307

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

A novel GYPA*01 allele with a c.125C > G (p.Thr42Ser) mutation identified in a Chinese individual.PMID 33682118Read ↗

A novel B allele with c.502C>G mutation identified in a Chinese individual.Semantic proximity Read ↗

Description of the first case of c.137-8C>T GYPB mutation not associated to the GYPB(P2) allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.145C>T variant.Semantic proximity Read ↗

Uncommon S-s-U+ phenotype encoded by two novel GYPB alleles.Semantic proximity Read ↗

A novel A allele with c.467C > T and c.784G > A nucleotide substitutions in Korean individuals.Semantic proximity Read ↗

A novel A allele with c.689G>T mutation identified in a Chinese individual.Semantic proximity Read ↗

A new allele with 303 base pairs insertion in B3GALT1 gene identified in an individual with P1 k phenotype.Semantic proximity Read ↗

A novel A allele with c.963_964insC mutation identified in a Chinese individual.Semantic proximity Read ↗

First report of a null allele on a GYPB*s background: GYPB*s(37 + 4_8delAGTGA).Semantic proximity Read ↗

A novel A allele with c.499G>A mutation identified in a Chinese individual.Semantic proximity Read ↗

A novel DO*01 silent allele associated with a nucleotide insertion in a Brazilian patient with anti-Gya.Semantic proximity Read ↗

A novel B allele with c.736T>C, c.738C>A, and c.930A>G variations identified in a Chinese individual with Bw phenotype.Semantic proximity Read ↗

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