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Article

A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Jul 2016

Kartal D, Borlu M, Has C, Fölster-Holst R

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Identifiers

PMID: 25865288
DOI: 10.1111/jdv.13163

Genes

FERMT1

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A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.PMID 25865288Read ↗

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

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Case of Kindler syndrome resulting from mutation in the FERMT1 gene.Semantic proximity Read ↗

A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome.Semantic 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 ↗

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

Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement.Semantic proximity Read ↗

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

Five new homozygous mutations in the KIND1 gene in Kindler syndrome.Semantic proximity Read ↗

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