Pung-amritt, P <br/><br/>
Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency.  [electronic resource] 

 -  Thrombosis and haemostasis  Feb 1999 
 - 189-92 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6245 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Blindness--etiology<br/>Codon--genetics<br/>DNA Mutational Analysis<br/>Disseminated Intravascular Coagulation--etiology<br/>Endophthalmitis--etiology<br/>Exons--genetics<br/>Female<br/>Fetal Diseases--etiology<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Heterozygote<br/>Humans<br/>IgA Vasculitis--congenital<br/>Infant, Newborn<br/>Point Mutation<br/>Protein S--genetics<br/>Protein S Deficiency--complications<br/>Retinal Vein Occlusion--embryology<br/>Risk Factors<br/>Thailand<br/>Thrombophilia--epidemiology