Marsella, Maria <br/><br/>
Characterization of Hb Calvino (HBB: c.406G > A): a new silent β-globin gene variant found in coexistence with α-thalassemia in a family of African origin.  [electronic resource] 

 -  Hemoglobin  2014 
 - 369-72 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1532-432X 
<br/><br/><label>Standard No.: </label>10.3109/03630269.2014.948186  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Angola--ethnology<br/>Child, Preschool<br/>Codon<br/>Fathers<br/>Female<br/>Gene Deletion<br/>Hemoglobins, Abnormal--analysis<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Italy<br/>Point Mutation<br/>Severity of Illness Index<br/>Siblings<br/>alpha-Thalassemia--blood<br/>beta-Globins--analysis