Channelpedia

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