Demirel, Nihal <br/><br/>
Severe purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation.  [electronic resource] 

 -  Pediatric hematology and oncology  Nov 2009 
 - 597-600 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1521-0669 
<br/><br/><label>Standard No.: </label>10.3109/08880010903116413  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Methylenetetrahydrofolate Reductase (NADPH2)--genetics<br/>Mutation<br/>Protein C Deficiency--genetics<br/>Purpura Fulminans--etiology