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Article

Case of Kindler syndrome resulting from mutation in the FERMT1 gene.

The Journal of dermatology - 1 Dec 2012

Wada Makoto, Masuda Koji, Tsuruta Daisuke, Tamai Katsuto, Lai-Cheong Joey E, McGrath John A, Katoh Norito

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Source

Identifiers

PMID: 22672060
DOI: 10.1111/j.1346-8138.2012.01598.x

Genes

FERMT1

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Case of Kindler syndrome resulting from mutation in the FERMT1 gene.PMID 22672060Read ↗

A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.Semantic proximity Read ↗

A novel mutation in the FERMT1 gene in a Spanish family with Kindler's syndrome.Semantic proximity Read ↗

The Kindler Syndrome: A Spectrum of FERMT1 Mutations in Iranian FamiliesSemantic proximity Read ↗

Novel Pathogenic Mutations of FERMT1 in two Chinese Kindler Syndrome FamiliesSemantic proximity Read ↗

Novel and recurrent FERMT1 gene mutations in Kindler syndrome.Semantic proximity Read ↗

Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.Semantic proximity Read ↗

[Clinical Characteristics and Gene Mutations in 186 Cases of Kindler Syndrome].Semantic proximity Read ↗

Kindler syndrome: report of two cases.Semantic proximity Read ↗

Kindler syndrome in a patient with colitis and primary sclerosing cholangitis: coincidence or association?Semantic proximity Read ↗

Two novel mutations in KIND1 in Indian patients with Kindler syndrome.Semantic proximity Read ↗

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