Freitas, Samuel da Silva <br/><br/>
Genetic variants of VWF gene in type 2 von Willebrand disease.  [electronic resource] 

 -  Haemophilia : the official journal of the World Federation of Hemophilia  Mar 2019 
 - e78-e85 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1365-2516 
<br/><br/><label>Standard No.: </label>10.1111/hae.13714  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA--chemistry<br/>Deamino Arginine Vasopressin--metabolism<br/>Exons<br/>Female<br/>Genetic Association Studies<br/>Genetic Variation<br/>Humans<br/>Male<br/>Middle Aged<br/>Polymorphism, Single Nucleotide<br/>Sequence Analysis, DNA<br/>Young Adult<br/>von Willebrand Disease, Type 2--genetics<br/>von Willebrand Factor--genetics