Santín, Sheila <br/><br/>
Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.  [electronic resource] 

 -  Kidney international  Dec 2009 
 - 1268-76 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1523-1755 
<br/><br/><label>Standard No.: </label>10.1038/ki.2009.381  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Amino Acid Substitution<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Female<br/>Genetic Association Studies<br/>Glomerulosclerosis, Focal Segmental--congenital<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Membrane Proteins--chemistry<br/>Mutation<br/>Mutation, Missense<br/>Nephrotic Syndrome--congenital<br/>Spain