Cabrera, Noelia <br/><br/>
Novel missense mutation c.2685G>C (p.Q895H) in VWF gene associated with very low levels of VWF mRNA.  [electronic resource] 

 -  Annals of hematology  Mar 2009 
 - 245-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-0584 
<br/><br/><label>Standard No.: </label>10.1007/s00277-008-0576-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Female<br/>Genetic Variation--genetics<br/>Humans<br/>Loss of Heterozygosity--genetics<br/>Male<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Phenotype<br/>RNA, Messenger--genetics<br/>von Willebrand Diseases--diagnosis<br/>von Willebrand Factor--genetics