Moret, A <br/><br/>
Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency.  [electronic resource] 

 -  Journal of thrombosis and thrombolysis  Nov 2019 
 - 674-678 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1573-742X 
<br/><br/><label>Standard No.: </label>10.1007/s11239-019-01911-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blood Coagulation Disorders, Inherited--genetics<br/>Codon, Nonsense<br/>Factor V--genetics<br/>Factor V Deficiency--genetics<br/>Genetic Variation<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Mutation<br/>Point Mutation