Mutation analysis of the CYLD gene in two Chinese families with multiple familial Trichoepithelioma
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-0960.2011.00763.x/fullpdf
Reference5 articles.
1. Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma;Zhang;J. Invest. Dermatol.,2004
2. Identification of the familial cylindromatosis tumour-suppressor gene;Bignell;Nat. Genet.,2000
3. A novel missense mutation in CYLD in a family with Brooke-Spiegler syndrome;Hu;J. Invest. Dermatol.,2003
4. CYLD mutation causes multiple familial trichoepithelioma in three Chinese families;Zheng;Hum. Mutat.,2004
5. CYLD is a deubiquitinatingenzyme that negatively regulates NF-kappaB activation by TNFR family members (see comment);Trompouki;Nature,2003
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1. Genetic Testing in CYLD Cutaneous Syndrome: An Update;The Application of Clinical Genetics;2021-10
2. The cylindromatosis (CYLD) gene and head and neck tumorigenesis;Cancers of the Head & Neck;2016-09-08
3. Phenotype–genotype correlations for clinical variants caused by CYLD mutations;European Journal of Medical Genetics;2015-05
4. A novel frameshift mutation in the cylindromatosis (CYLD) gene in a Chinese family with multiple familial trichoepithelioma;Archives of Dermatological Research;2014-09-19
5. Germline mutation analysis in the CYLD gene in Chinese patients with multiple trichoepitheliomas;Genetics and Molecular Research;2014
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