Brenner, B <br/><br/>
Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis.  [electronic resource] 

 -  Blood  Aug 1996 
 - 877-80 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Consanguinity<br/>Disease Susceptibility<br/>Factor V--genetics<br/>Factor V Deficiency--genetics<br/>Female<br/>Genetic Heterogeneity<br/>Heterozygote<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Pedigree<br/>Protein C--genetics<br/>Thrombophlebitis--genetics<br/>Thrombosis--congenital