c.543G>C mutation in ABO*A.1.02 allele responsible for a weak A phenotype-Reference-Cited by-同舟云学术

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c.543G>C mutation in ABO*A.1.02 allele responsible for a weak A phenotype

Published:2019-07 Issue:8 Volume:59 Page:2756-2757
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Yang Xiaojun¹^ORCID,Ma Shuqun²,Xie Haihua³,Sun Jiafeng³,Chen Liangyuan¹,Chen Fawen¹³

Affiliation:

1. Department of Transfusion Medicine Clinical College of Fujian Provincial Hospital, Fujian Medical University Fuzhou China

2. Department of Transfusion Medicine Fuqing Hospital Fuzhou China

3. Department of Clinical Laboratory Fujian Provincial Jinshan Hospital Fuzhou China

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15430

Reference4 articles.

1. Molecular genetic analysis for the Bxsubgroup revealing two novel alleles in the ABO gene

2. DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach

3. The structural basis for specificity in human ABO(H) blood group biosynthesis

4. Molecular genetic analysis for Ax phenotype of the ABO blood group system in Chinese

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. c.586T>C mutation on the ABO*A1.02 allele responsible for A _el phenotype;Transfusion;2022-04-26

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