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Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations.
Okano, Tsubasa; Nishimura, Akira; Inoue, Kento; Naruto, Takuya; Tokoro, Shown; Tomoda, Takahiro; Kamiya, Takahiro; Simbo, Asami; Akutsu, Yuko; Okamoto, Keisuke; Yeh, Tzuwen; Isoda, Takeshi; Yanagimachi, Masakatsu; Kajiwara, Michiko; Imai, Kohsuke; Kanegane, Hirokazu; Mori, Masaaki; Morio, Tomohiro; Takagi, Masatoshi.
  • Okano T; Department of Pediatrics and Developmental Biology.
  • Nishimura A; Department of Pediatrics and Developmental Biology.
  • Inoue K; Department of Pediatrics and Developmental Biology.
  • Naruto T; Department of Lifetime Clinical Immunology.
  • Tokoro S; Department of Dermatology, Graduate School of Medical and Dental Sciences.
  • Tomoda T; Department of Pediatrics and Developmental Biology.
  • Kamiya T; Department of Pediatrics and Developmental Biology.
  • Simbo A; Department of Pediatrics and Developmental Biology.
  • Akutsu Y; Department of Pediatrics and Developmental Biology.
  • Okamoto K; Department of Pediatrics and Developmental Biology.
  • Yeh T; Department of Pediatrics and Developmental Biology.
  • Isoda T; Department of Pediatrics and Developmental Biology.
  • Yanagimachi M; Department of Pediatrics and Developmental Biology.
  • Kajiwara M; Center for Transfusion Medicine and Cell Therapy, Medical Hospital.
  • Imai K; Department of Pediatrics, Perinatal and Maternal Medicine.
  • Kanegane H; Department of Child Health and Development, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Mori M; Department of Lifetime Clinical Immunology.
  • Morio T; Department of Pediatrics and Developmental Biology.
  • Takagi M; Department of Pediatrics and Developmental Biology.
Rheumatology (Oxford) ; 60(12): e429-e431, 2021 12 01.
Article en En | MEDLINE | ID: mdl-34528076
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / ADN / Dermatitis / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Mutación Tipo de estudio: Diagnostic_studies Límite: Child / Child, preschool / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / ADN / Dermatitis / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Mutación Tipo de estudio: Diagnostic_studies Límite: Child / Child, preschool / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article