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NeMO mutations: a rare cause of monogenic Behçet-like disease.
Baldini, Letizia; Di Sabatino, Fabiana; Bodrero, Enrico; Dellepiane, Marta; Covizzi, Carlotta; La Selva, Roberta; Montin, Davide; Licciardi, Francesco.
Afiliación
  • Baldini L; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
  • Di Sabatino F; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
  • Bodrero E; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
  • Dellepiane M; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
  • Covizzi C; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
  • La Selva R; Unit of Pediatric Plastic Surgery, Pediatric Dermatology, Città della Salute e della Scienza di Torino, Regina Margherita Children Hospital, Turin, Italy.
  • Montin D; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
  • Licciardi F; Department of Pediatrics and Public Health, University of Turin, Turin, Italy.
Rheumatology (Oxford) ; 60(3): e92-e94, 2021 03 02.
Article en En | MEDLINE | ID: mdl-32954429
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Behçet / Quinasa I-kappa B Límite: Child, preschool / Female / Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de Behçet / Quinasa I-kappa B Límite: Child, preschool / Female / Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Italia