Tanha, N <br/><br/>
MBL2 gene variants coding for mannose-binding lectin deficiency are associated with increased risk of nephritis in Danish patients with systemic lupus erythematosus.  [electronic resource] 

 -  Lupus  Oct 2014 
 - 1105-11 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1477-0962 
<br/><br/><label>Standard No.: </label>10.1177/0961203314536478  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Alleles<br/>Child<br/>Denmark--epidemiology<br/>Female<br/>Follow-Up Studies<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Genotype<br/>Humans<br/>Lupus Erythematosus, Systemic--complications<br/>Lupus Nephritis--epidemiology<br/>Male<br/>Mannose-Binding Lectin--deficiency<br/>Metabolism, Inborn Errors--genetics<br/>Middle Aged<br/>Proportional Hazards Models<br/>Regression Analysis<br/>Risk Factors<br/>Young Adult