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Article

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

20 Dec 2009

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 20023659
DOI: 10.1038/ng.505

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Click a neighbor to travelStep 1 · 12 closest

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosisPMID 20023659Read ↗

Clinical and Pathological Heterogeneity in FSGS due to INF2 MutationsSemantic proximity Read ↗

Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.Semantic proximity Read ↗

[Case report; A case of familial focal segmental glomerulosclerosis with a mutation in the formin INF2].Semantic proximity Read ↗

Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.Semantic proximity Read ↗

The formin INF2 in disease: progress from 10 years of research.Semantic proximity Read ↗

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.Semantic proximity Read ↗

Autosomal dominant focal segmental glomerulosclerosis by INF2 p.Arg218Trp and p.Ser186Pro mutations: three case reports and literature review.Semantic proximity Read ↗

Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome.Semantic proximity Read ↗

Role of formin INF2 in human diseases.Semantic proximity Read ↗

INF2 mutations cause kidney disease through a gain-of-function mechanism.Semantic proximity Read ↗

Variable renal phenotype in a family with an INF2 mutation.Semantic proximity Read ↗

Missense Mutant Gain-of-Function Causes Inverted Formin 2 (INF2)-Related Focal Segmental Glomerulosclerosis (FSGS)Semantic proximity Read ↗

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