Bresin, Elena <br/><br/>
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.  [electronic resource] 

 -  Journal of the American Society of Nephrology : JASN  Feb 2013 
 - 475-86 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1533-3450 
<br/><br/><label>Standard No.: </label>10.1681/ASN.2012090884  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Atypical Hemolytic Uremic Syndrome<br/>Child<br/>Child, Preschool<br/>Complement C3--genetics<br/>Complement Factor B--genetics<br/>Complement Factor H--genetics<br/>Complement System Proteins--genetics<br/>Female<br/>Fibrinogen--genetics<br/>Genetic Association Studies<br/>Haplotypes<br/>Hemolytic-Uremic Syndrome--genetics<br/>Humans<br/>Infant<br/>Male<br/>Membrane Cofactor Protein--genetics<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Penetrance<br/>Risk Factors<br/>Young Adult