A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis-Reference-Cited by-同舟云学术

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis

Published:2019-05 Issue:5 Volume:139 Page:1195-1198
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Vahidnezhad Hassan,Youssefian Leila,Saeidian Amir Hossein,Mansoori Behzad,Jazayeri Ali,Azizpour Arghavan,Hesari Kambriz Kamyab,Yousefi Mehdi,Zeinali Sirous,Jouanguy Emmanuelle,Casanova Jean-Laurent,Uitto Jouni

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

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3. The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses;de Jong;J Exp Med,2018

4. Estimating the age of rare disease mutations: the example of Triple-A syndrome;Genin;J Med Genet,2004

5. A novel approach to the classification of epidermodysplasia verruciformis;Huang;Int J Dermatol,2018

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