A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression-Reference-Cited by-同舟云学术

A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression

Published:2017-07 Issue:1 Volume:101 Page:130-138
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Chen Diyu,Zuo Yangjin,Zhang Xinhua,Ye Yuhua,Bao Xiuqin,Huang Haiyan,Tepakhan Wanicha,Wang Lijuan,Ju Junyi,Chen Guangfu,Zheng Mincui,Liu Dun,Huang Shuodan,Zong Lu,Li Changgang,Chen Yajun,Zheng Chenguang,Shi Lihong,Zhao Quan,Wu Qiang,Fucharoen Supan,Zhao Cunyou,Xu Xiangmin

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference25 articles.

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2. Thalassaemia;Higgs;Lancet,2012

3. Genetic association studies in β-hemoglobinopathies;Thein;Hematology (Am Soc Hematol Educ Program),2013

4. Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A;Sankaran;Science,2008

5. KLF1 regulates BCL11A expression and gamma- to beta-globin gene switching;Zhou;Nat. Genet.,2010

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