Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency is a research paper published in Viruses (2024). On theSindex it has a DataRank of 0. It has been cited 2 times.
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Laboratory of Clinical Immunology—Inflammation and Allergy (LICIA), Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco
Grant: R01AI143810
Laboratory of Clinical Immunology—Inflammation and Allergy (LICIA), Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco
Grant: UL1TR001866
Laboratory of Clinical Immunology—Inflammation and Allergy (LICIA), Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco
Grant: ANR-10-IAHU-01
Laboratory of Clinical Immunology—Inflammation and Allergy (LICIA), Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco
Grant: ANR-10-LABX-62-IBEID
National Institutes of Health
Grant: 5UL1TR001866-07
Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational Success
National Institutes of Health
Grant: 5R01AI143810-03
Molecular and cellular basis of epidermodysplasia verruciformis
Institut National de la Santé et de la Recherche Médicale (INSERM)
Square Foundation
Howard Hughes Medical Institute, the Rockefeller University
MD-PhD program of Imagine Institute
National Center for Advancing Translational Sciences (NCATS)
Laboratory of Clinical Immunology—Inflammation and Allergy (LICIA), Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, Morocco
St. Giles Foundation
University of Paris Cité
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