Koda, Y <br/><br/>
Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system.  [electronic resource] 

 -  Biochemical and biophysical research communications  Sep 1997 
 - 21-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-291X 
<br/><br/><label>Standard No.: </label>10.1006/bbrc.1997.7232  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ABO Blood-Group System--genetics<br/>Alleles<br/>Animals<br/>COS Cells<br/>Fucosyltransferases--deficiency<br/>Humans<br/>Mutation<br/>Phenotype<br/>Sequence Deletion<br/>Galactoside 2-alpha-L-fucosyltransferase