Familial FSGS
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference54 articles.
1. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis;Brown;Nat Genet,2010
2. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis;Gbadegesin;Kidney Int,2012
3. Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis;Boyer;J Am Soc Nephrol,2011
4. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis;Barua;Kidney Int,2013
5. INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy;Boyer;N Engl J Med,2011
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