Mahdieh, Nejat <br/><br/>
Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East.  [electronic resource] 

 -  Blood reviews  11 2016 
 - 493-508 p.  digital 
<br/><br/> Publication Type: Journal Article; Meta-Analysis; Review 
<br/><br/><label>ISSN: </label>1532-1681 
<br/><br/><label>Standard No.: </label>10.1016/j.blre.2016.07.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Binding Sites<br/>Computational Biology--methods<br/>DNA Mutational Analysis<br/>Ethnicity--genetics<br/>Genetic Association Studies<br/>Humans<br/>Iran--epidemiology<br/>Middle East--epidemiology<br/>Models, Molecular<br/>Mutation<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Population Surveillance<br/>Protein Binding<br/>Protein Conformation<br/>Protein Interaction Mapping<br/>Protein Interaction Maps<br/>Structure-Activity Relationship<br/>beta-Globins--chemistry<br/>beta-Thalassemia--epidemiology