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Article

A novel nonsense mutation of the CYLD gene in a Turkish family with multiple familial trichoepithelioma.

Clinical and experimental dermatology - 1 Jun 2020

Sarikaya Solak S, Yalcıntepe S, Atahan C, Nagy N, Can N

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Share to Child
Share to Codon, Nonsense
Share to Deubiquitinating Enzyme CYLD
Share to Neoplastic Syndromes, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31833565
DOI: 10.1111/ced.14144

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

Related research

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A novel nonsense mutation of the CYLD gene in a Turkish family with multiple familial trichoepithelioma.PMID 31833565Read ↗

Three mutations of CYLD gene in Chinese families with multiple familial trichoepithelioma.Semantic proximity Read ↗

Multiple familial trichoepithelioma with a novel mutation of the CYLD gene.Semantic proximity Read ↗

Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China.Semantic proximity Read ↗

A novel mutation of CYLD in a Chinese family with multiple familial trichoepithelioma.Semantic proximity Read ↗

Multiple familial trichoepithelioma: report of a Chinese family not associated with a mutation in the CYLD gene and CYLD protein expression in the trichoepithelioma tumor tissue.Semantic proximity Read ↗

A novel splicing mutation of the CYLD gene in a Taiwanese family with multiple familial trichoepithelioma.Semantic proximity Read ↗

A novel frameshift mutation in the cylindromatosis (CYLD) gene in a Chinese family with multiple familial trichoepithelioma.Semantic proximity Read ↗

Multiple trichoepitheliomas--a novel mutation in the CYLD gene.Semantic proximity Read ↗

[Multiple familial trichoepithelioma: a new CYLD gene mutation].Semantic proximity Read ↗

Phenotype variability in tumor disorders of the skin appendages associated with mutations in the CYLD gene.Semantic proximity Read ↗

A novel missense mutation in CYLD in a family with Brooke-Spiegler syndrome.Semantic proximity Read ↗

Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation.Semantic proximity Read ↗

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