A new missense mutation c.692C>A caused a weak Ael phenotype in a Chinese individual-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A new missense mutation c.692C>A caused a weak Ael phenotype in a Chinese individual

Published:2019-10 Issue:10 Volume:59 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Yu Shuhong¹,Feng Zhihui²^ORCID,Ma Wenhui²^ORCID,Yan Ping³

Affiliation:

1. Department of Blood TransfusionYan Tai Yuhuangding Hospital Yantai China

2. Institute for Transfusion Medicine, Qingdao Blood Center Qingdao China

3. Clinical LaboratoryQingdao Hicer Medical Group Qingdao China

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15503

Reference3 articles.

1. Cloning and characterization of DNA complementary to human UDP–GalNac: fucal2GalNac transferase mRNA;Yamamoto F;J Biol Chem,1990

2. A novel A allele with c.689G>T mutation identified in a Chinese individual

3. Prediction of deleterious human alleles

Cited by 3 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. ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype;Transfusion;2021-07-29

2. A novel A allele with c.963_964insC mutation identified in a Chinese individual;Transfusion;2020-11-04

3. A novel A allele with c. 499G >A mutation identified in a Chinese individual;Transfusion;2020-04-24

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP