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Ichthyosis follicularis syndromes in patients with mutations in GJB2.
Youssefian, Leila; Naji, Mahtab; Park, Jason S; Rajabi, Fateme; Abdollahimajd, Fahimeh; Mahmoudi, Hamidreza; Kamyab-Hesari, Kambiz; Ghalamkarpour, Fariba; Zabihi, Masoud; Teimoorian, Mehrdad; Youssefian, Laya; Zeinali, Sirous; Vahidnezhad, Hassan; Uitto, Jouni.
Afiliação
  • Youssefian L; Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
  • Naji M; Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, PA, USA.
  • Park JS; Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
  • Rajabi F; Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
  • Abdollahimajd F; Geisinger Commonwealth School of Medicine, Scranton, PA, USA.
  • Mahmoudi H; Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Kamyab-Hesari K; Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Ghalamkarpour F; Department of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
  • Zabihi M; Department of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
  • Teimoorian M; Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Youssefian L; Stem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
  • Zeinali S; Stem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
  • Vahidnezhad H; ENT and Head & Neck Research Center, The Five Senses Institute, Iran University of Medical Sciences, Tehran, Iran.
  • Uitto J; Kawsar Human Genetics Research Center, Tehran, Iran.
Clin Exp Dermatol ; 47(8): 1561-1566, 2022 Aug.
Article em En | MEDLINE | ID: mdl-35396755
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Surdez / Conexina 26 / Perda Auditiva Neurossensorial / Ictiose Limite: Humans Idioma: En Revista: Clin Exp Dermatol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Surdez / Conexina 26 / Perda Auditiva Neurossensorial / Ictiose Limite: Humans Idioma: En Revista: Clin Exp Dermatol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos