Identification of a novel missense variant (<scp>c.567G</scp>><scp>A</scp>, <scp>p. Met189Ile</scp>) in <i>ABO*B.01</i> allele

Authors

Xiu‐Qing Li (ORCID: https://orcid.org/0000-0002-7308-0596)
Yunxiang Wu
Fei Wang (ORCID: https://orcid.org/0000-0001-6769-8309)
Hua Wang (ORCID: https://orcid.org/0009-0000-2039-1051)
Zhicheng Li (ORCID: https://orcid.org/0000-0002-5271-3753)
Yajun Liang (ORCID: https://orcid.org/0000-0001-5236-2095)
Yi Xu
D.X. Zhang (ORCID: https://orcid.org/0009-0004-2225-1633)
Ruiqing Guo
J. X. Zuo

Publication Details

Journal: Transfusion
Published: 2025-02-22
DOI: https://doi.org/10.1111/trf.18175
Primary Topic: Blood groups and transfusion
Type: article
Field-Weighted Citation Impact: 0.00

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article

Identification of a novel missense variant (c.567G>A, p. Met189Ile) in ABOB.01* allele

Xiu‐Qing Li, Yunxiang Wu, Fei Wang, Hua Wang et al.

Feb 22, 2025

Transfusion

Blood groups and transfusion

article

Identification of a novel missense variant (c.567G>A, p. Met189Ile) in ABOB.01* allele

Xiu‐Qing Li, Yunxiang Wu, Fei Wang, Hua Wang, Zhicheng Li, Yajun Liang, Yi Xu, D.X. Zhang, Ruiqing Guo, J. X. Zuo

February 22, 2025article en

Abstract

No abstract available for this paper.

TransfusionVol. 65(4)

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Openalex Percentile: Top 96%

Blood groups and transfusion

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Identification of a novel missense variant (<scp>c.567G</scp>><scp>A</scp>, <scp>p. Met189Ile</scp>) in <i>ABO*B.01</i> allele — Xiu‐Qing Li, Yunxiang Wu, et al. · Transfusion (2025) | TGRS Research Map | TGRS

Identification of a novel missense variant (<scp>c.567G</scp>&gt;<scp>A</scp>, <scp>p. Met189Ile</scp>) in <i>ABO*B.01</i> allele

Authors

Publication Details

Identification of a novel missense variant (c.567G>A, p. Met189Ile) in ABO*B.01 allele

Identification of a novel missense variant (c.567G>A, p. Met189Ile) in ABO*B.01 allele

Abstract

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Identification of a novel missense variant (<scp>c.567G</scp>><scp>A</scp>, <scp>p. Met189Ile</scp>) in <i>ABO*B.01</i> allele

Identification of a novel missense variant (c.567G>A, p. Met189Ile) in ABOB.01* allele

Identification of a novel missense variant (c.567G>A, p. Met189Ile) in ABOB.01* allele