Identification of LCK mutation in a family with atypical epidermodysplasia verruciformis with T-cell defects and virus-induced squamous cell carcinoma

Summary Background Inherited epidermodysplasia verruciformis (EV) is a rare skin disorder characterized by susceptibility to specific types of human papilloma virus (HPV) and is strongly associated with skin carcinomas. Inactivating mutations in EVER1/EVER2 account for most cases of EV. However, mor...

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Veröffentlicht in:	British journal of dermatology (1951) 2016-12, Vol.175 (6), p.1204-1209
Hauptverfasser:	Li, S.-L., Duo, L.-N., Wang, H.-J., Dai, W., Zhou, E.-Y.H., Xu, Y.-N., Zhao, T., Xiao, Y.-Y., Xia, L., Yang, Z.-H., Zheng, L.-T., Hu, Y.-Y., Lin, Z.-M., Wang, H.-N., Gao, T.-W., Ma, C.-L., Yang, Y., Li, C.-Y.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent DNA, Recombinant - genetics Epidermodysplasia Verruciformis - genetics Female Homozygote Humans Lymphocyte Specific Protein Tyrosine Kinase p56(lck) - metabolism Male Mutation - genetics Papillomavirus Infections - genetics Pedigree Skin Diseases - genetics Young Adult
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