Fu, Q <br/><br/>
Type I coagulation factor V deficiency caused by compound heterozygous mutation of F5 gene.  [electronic resource] 

 -  Haemophilia : the official journal of the World Federation of Hemophilia  Sep 2003 
 - 646-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1351-8216 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2516.2003.00800.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Base Sequence<br/>DNA Mutational Analysis--methods<br/>DNA, Complementary--genetics<br/>Factor V--genetics<br/>Factor V Deficiency--genetics<br/>Female<br/>Humans<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree