Fucharoen, S <br/><br/>
A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe.  [electronic resource] 

 -  British journal of haematology  Jul 1990 
 - 393-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.1990.tb04354.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Blotting, Southern<br/>Chromosome Deletion<br/>Codon<br/>DNA--analysis<br/>Globins--genetics<br/>Humans<br/>Inclusion Bodies--pathology<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation<br/>Thalassemia--blood