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Article

c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype.

Transfusion - 1 Oct 2018

Li Xiaofei, Li Aijun, Xia Xiaoye, Wang Deqing, Zhu Faming

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 30204935
DOI: 10.1111/trf.14928

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype.PMID 30204935Read ↗

A new missense variant c.278C > G on the ABO*B.01 allele associated with a Bel phenotype.Semantic proximity Read ↗

The novel missense variant c.350G>T on the ABO*B.01 allele associated with a Bel phenotype.Semantic proximity Read ↗

Identification of a novel missense mutation (563G>a) in the ABO gene associated with a Bel phenotype.Semantic proximity Read ↗

Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.Semantic proximity Read ↗

Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.Semantic proximity Read ↗

Identification of a novel B allele with a c.917 T > C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.Semantic proximity Read ↗

Identification of a novel A allele with a c.423 C > A mutation on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.Semantic proximity Read ↗

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