Multiple rare genetic variants co-segregating with familial IgA nephropathy all act within a single immune-related network
Academic Article
Publication Date:
2016
abstract:
Background. IgA nephropathy (IgAN) is a common complex disease with a strong genetic involvement. We aimed to identify novel, rare, highly penetrant risk variants combining family-based linkage analysis with whole-exome sequencing (WES).
Iris type:
01.01 Articolo in rivista
Keywords:
familymedicine; genepolymorphism; genetics; glomerulonephritis; kidney disease
List of contributors:
Ancona, Nicola
Published in: