A KLF1 gene mutation causes β-thalassemia minor in a Chinese family-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A KLF1 gene mutation causes β-thalassemia minor in a Chinese family

Published:2018-02-02 Issue:2 Volume:40 Page:e35-e37
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Huang L.-Y.¹,Li J.¹,Zhang Y.²,Li D.-Z.¹^ORCID

Affiliation:

1. Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University; Guangzhou Guangdong China

2. Euler Genomics; Beijing China

Funder

Guangdong Provincial Department of Science and Technology Agency

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12788/fullpdf

Reference12 articles.

1. The multifunctional role of EKLF/KLF1 during erythropoiesis;Siatecka;Blood,2011

2. Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants;Perkins;Blood,2016

3. Lethal beta-thalassaemia in mice lacking the erythroid ACCC-transcription factor EKLF;Perkins;Nature,1995

4. A new Krüppel-like factor 1 mutation (c.947G>AA or p. C316Y) in humans causes β-thalassemia minor;Nitta;Hemoglobin,2015

5. Prenatal control of severe thalassaemia: Chiang Mai strategy;Tongsong;Prenat Diagn,2000

Cited by 2 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. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

2. Krüppel-Like Factor 1Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia;Hemoglobin;2019-01-02

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

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3