A novel mutation of CYLD in a Chinese family with multiple familial trichoepithelioma
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2011.04309.x/fullpdf
Reference28 articles.
1. Sporadic trichoepithelioma demonstrates deletions at 9q22.3;Matt;Arch Dermatol,2000
2. Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma;Zhang;J Invest Dermatol,2004
3. Mutations in the CYLD gene in Brooke-Spiegler syndrome, familial cylindromatosis, and multiple familial trichoepithelioma: lack of genotype-phenotype correlation;Bowen;J Invest Dermatol,2005
4. Phenotype diversity in familial cylindromatosis: a frameshift mutation in the tumor suppressor gene CYLD underlies different tumors of skin appendages;Poblete Gutierrez;J Invest Dermatol,2002
5. CYLD mutations underlie Brooke-Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes;Young;Clin Genet,2006
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1. Genetic Testing in CYLD Cutaneous Syndrome: An Update;The Application of Clinical Genetics;2021-10
2. Can we clinically identify patients at risk of malignant transformation of skin tumors in Brooke–Spiegler syndrome?;Acta Dermatovenerologica Alpina Pannonica et Adriatica;2020
3. Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family;The Journal of Dermatology;2019-02-27
4. An extremely rare association of multiple familial trichoepitheliomas and hereditary multiple osteochondromas;International Journal of Dermatology;2018-09-23
5. The cylindromatosis (CYLD) gene and head and neck tumorigenesis;Cancers of the Head & Neck;2016-09-08
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