PubMed 23014460
Referenced in: none
Automatically associated channels: Kir2.3 , TRP , TRPC , TRPC6
Title: Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.
Authors: Moumita Barua, Elizabeth J Brown, Victoria T Charoonratana, Giulio Genovese, Hua Sun, Martin R Pollak
Journal, date & volume: Kidney Int., 2013 Feb , 83, 316-22
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23014460
Abstract