Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3

IgA nephropathy (IgAN) is not generally considered a hereditary disease, even though extensive evidence suggests an undefined genetic influence. Linkage analysis identified a number of genome regions that could contain variations linked to IgAN. In this case-control association study, genes possibly...

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Veröffentlicht in:	Nephrology, dialysis, transplantation dialysis, transplantation, 2012-06, Vol.27 (6), p.2328-2337
Hauptverfasser:	BERTINETTO, Francesca Eleonora, CALAFELL, Francesc, PAOLO SCHENA, Francesco, AMOROSO, Antonio, ROGGERO, Stefano, CHIDICHIMO, Rossella, GARINO, Elena, MARCUCCIO, Cristina, COPPO, Rosanna, SCOLARI, Francesco, FRASCA, Giovanni Maria, SAVOIDL, Silvana
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Biomarkers - analysis Case-Control Studies Child Child, Preschool Chromosome Mapping Emergency and intensive care: renal failure. Dialysis management Female Genetic Linkage Genetic Predisposition to Disease Genotype Glomerulonephritis Glomerulonephritis, IGA - genetics Glomerulonephritis, IGA - pathology Humans Infant Intensive care medicine Male Medical sciences Middle Aged Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Polymorphism, Single Nucleotide - genetics Prognosis Proteinuria - genetics Proteinuria - pathology Retrospective Studies Survival Rate Young Adult
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