A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes.

Mohamad, Janan; Sarig, Ofer; Beattie, Paula; Malovitski, Kiril; Assaf, Sari; O'Toole, Edel; Schwartz, Janice; Evans, Holly; Samuelov, Liat; Sprecher, Eli

Mohamad, Janan; Sarig, Ofer; Beattie, Paula; Malovitski, Kiril; Assaf, Sari; O'Toole, Edel; Schwartz, Janice; Evans, Holly; Samuelov, Liat; Sprecher, Eli.

Afiliación

Mohamad J; Division of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Sarig O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Beattie P; Division of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Malovitski K; Department of Dermatology, Royal Hospital for Children, Glasgow, UK.
Assaf S; Division of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
O'Toole E; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Schwartz J; Division of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Evans H; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Samuelov L; Blizard Institute, Faculty of Medicine and Dentistry, Queen Mary University of London, London, UK.
Sprecher E; Department of Dermatology, The Royal London Hospital, London, UK.

Br J Dermatol ; 187(5): 773-777, 2022 11.

Article en En | MEDLINE | ID: mdl-35822506

Asunto(s)

Queratina-17; Queratinas; Queratina-17/genética; Heterocigoto; Fenotipo; Citoesqueleto; Mutación; Queratina-6/genética; Queratina-14/genética; Queratina-16

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Queratina-17 / Queratinas Tipo de estudio: Prognostic_studies Idioma: En Revista: Br J Dermatol Año: 2022 Tipo del documento: Article País de afiliación: Israel

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