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Article

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

Transfusion - 1 Sept 2022

Deng Danfei, Deng Gang, He Yunlei, Yu Yong

Abstract excerpt

No abstract is available from the source.

Topics

ABO Blood-Group System
Alleles
Exons
Genotype
Humans
Mutation
Mutation, Missense
Phenotype

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 35916252
DOI: 10.1111/trf.17041

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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