IgA nephropathy type 2
IgA nephropathy type 2 is a probably autosomal dominant disorder associated with genetic alterations at chromosome positions 4q26-q31 and 17q12-q22. The exact genes are not yet discovered.
|IgA nephropathy type 1|
|IgA nephropathy type 2|
|IgA nephropathy type 3|
Bisceglia L et al. (2006) Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci.[^]
Paterson AD et al. (2007) Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.[^]
OMIM.ORG articleOmim 613944 [^]