Harteveld, Cornelis L <br/><br/>
Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.  [electronic resource] 

 -  Hemoglobin  2007 
 - 325-32 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0363-0269 
<br/><br/><label>Standard No.: </label>10.1080/03630260701459374  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Globins--genetics<br/>Hemoglobins, Abnormal--chemistry<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Protein Conformation<br/>Thalassemia--genetics