CYLD-related cutaneous syndrome: variable p.Pro482fs*6 phenotype in five individuals from two unrelated families

J Eur Acad Dermatol Venereol. 2021 Jan;35(1):e81-e83. doi: 10.1111/jdv.16823. Epub 2020 Aug 11.

D Carton de Tournai^{1

2}, I Vandernoot^{1

3}, M Marangoni³, D Faverly⁴, M Diaz⁵, A Casagranda¹, E Berlingin¹, L Van Maldergem^{6

7}

¹ Department of Dermatology, Ambroise Paré University Hospital, Mons, Belgium.
² Department of Dermatology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
³ Center of Human Genetics, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
⁴ Center of Morphological Pathology, Brussels, Belgium.
⁵ Department of Oncology, Ambroise Paré University Hospital, Mons, Belgium.
⁶ Clinical Investigation Center 1431, National Institute of Health and Medical Research (INSERM), Paris, France.
⁷ Center of Human Genetics, University of Franche-Comté, Besançon, France.

No abstract available

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