Wester, Elisabet S <br/><br/>
Genetic basis of the K(0) phenotype in the Swedish population.  [electronic resource] 

 -  Transfusion  Apr 2005 
 - 545-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0041-1132 
<br/><br/><label>Standard No.: </label>10.1111/j.0041-1132.2005.04283.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Alternative Splicing<br/>Codon, Nonsense--genetics<br/>Family Health<br/>Female<br/>Genetics, Population<br/>Humans<br/>Introns<br/>Kell Blood-Group System--genetics<br/>Male<br/>Pedigree<br/>Phenotype<br/>Point Mutation<br/>Sweden