Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.

Journal of the peripheral nervous system : JPNS - 1 Mar 2013

Toyota Kentaro, Ogino Daisuke, Hayashi Makiko, Taki Masashi, Saito Kayoko, Abe Akiko, Hashimoto Taeko, Umetsu Kazuo, Tsukaguchi Hiroyasu, Hayasaka Kiyoshi

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Charcot-Marie-Tooth Disease
Share to Child
Share to Formins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glomerulosclerosis, Focal Segmental

Share to Microfilament Proteins

Share to Mutation

Source

Identifiers

PMID: 23521651
DOI: 10.1111/jns5.12014

Genes

INF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.PMID 23521651Read ↗

INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.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 ↗

A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.Semantic proximity Read ↗

De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy.Semantic proximity Read ↗

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

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.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 ↗

Novel INF2 mutation p. L77P in a family with glomerulopathy and Charcot-Marie-Tooth neuropathy.Semantic proximity Read ↗

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

Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.Semantic proximity Read ↗

A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis.Semantic proximity Read ↗

INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.