Associated Papers
Genetic Testing in CYLD Cutaneous Syndrome: An Update.
Nagy N et al.
The Application of Clinical Genetics, 2021
Phenotype variability in tumor disorders of the skin appendages associated with mutations in the CYLD gene.
Parren LJMT et al.
Archives of Dermatological Research, 2018
Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation.
Tantcheva-Poór I et al.
Dermatology (basel, Switzerland), 2016
The cylindromatosis (CYLD) gene and head and neck tumorigenesis.
Verhoeft KR et al.
Cancers of the Head & Neck, 2016
Novel and recurrent germline and somatic mutations in a cohort of 67 patients from 48 families with Brooke-Spiegler syndrome including the phenotypic variant of multiple familial trichoepitheliomas and correlation with the histopathologic findings in 379 biopsy specimens.
Grossmann P et al.
The American Journal of Dermatopathology, 2013
A novel missense mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.
Wang FX et al.
Archives of Dermatological Research, 2010
Update of cylindromatosis gene (CYLD) mutations in Brooke-Spiegler syndrome: novel insights into the role of deubiquitination in cell signaling.
Blake PW et al.
Human Mutation, 2009
Novel substitution and frameshift mutations of CYLD in two Chinese families with multiple familial trichoepithelioma.
Liang YH et al.
The British Journal of Dermatology, 2008
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