Viprakasit, Vip <br/><br/>
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.  [electronic resource] 

 -  Blood  Mar 2014 
 - 1586-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-0020 
<br/><br/><label>Standard No.: </label>10.1182/blood-2013-09-526087  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amino Acid Sequence<br/>Anemia, Hemolytic--blood<br/>Child<br/>Child, Preschool<br/>Conserved Sequence<br/>Erythrocyte Indices<br/>Erythrocytes--metabolism<br/>Female<br/>Fetal Hemoglobin--chemistry<br/>Gene Expression Regulation<br/>Gene Order<br/>Humans<br/>Infant<br/>Kruppel-Like Transcription Factors--genetics<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Protein Binding<br/>Protein Interaction Domains and Motifs<br/>Sequence Alignment<br/>Transfusion Reaction<br/>Young Adult<br/>alpha-Globins--metabolism<br/>beta-Globins--metabolism