Raffield, Laura M <br/><br/>
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.  [electronic resource] 

 -  PLoS genetics  03 2018 
 - e1007293 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1553-7404 
<br/><br/><label>Standard No.: </label>10.1371/journal.pgen.1007293  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Black or African American<br/>Anemia, Sickle Cell--blood<br/>Cohort Studies<br/>DNA Copy Number Variations<br/>Erythrocytes, Abnormal<br/>Glomerular Filtration Rate<br/>Glycated Hemoglobin--metabolism<br/>Hemoglobin, Sickle--genetics<br/>Humans<br/>Phenotype<br/>Sickle Cell Trait<br/>Young Adult<br/>alpha-Globins--genetics<br/>alpha-Thalassemia--genetics