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Article

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

Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine - 10 May 2013

Yamamoto Junya, Nakazawa Daigo, Tsukaguchi Hiroyasu, Toyoyama Takayuki, Sato Akiko, Nakagaki Tasuku, Ishikawa Yasunobu, Shibazaki Sekiya, Nishio Saori, Atsumi Tatsuya

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Identifiers

PMID: 23847988
DOI: 10.2169/naika.102.1220

Genes

INF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Case report; A case of familial focal segmental glomerulosclerosis with a mutation in the formin INF2].PMID 23847988Read ↗

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosisSemantic proximity Read ↗

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

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

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

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

Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.Semantic proximity Read ↗

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

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.Semantic proximity Read ↗

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

Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.Semantic proximity Read ↗

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