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Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome.
Chang, Shao-Yu; Kambe, Naotomo; Fan, Wen-Lang; Huang, Jing-Long; Lee, Wen-I; Wu, Chao-Yi.
Afiliação
  • Chang SY; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Kambe N; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Fan WL; Genomic Medicine Research Core Laboratory, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Huang JL; Department of Medical Research, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
  • Lee WI; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Wu CY; Division of Allergy, Asthma, and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital, No.5 Fu-Hsing St., Taoyuan, Taiwan, R.O.C.
Pediatr Rheumatol Online J ; 20(1): 86, 2022 Oct 03.
Article em En | MEDLINE | ID: mdl-36192768
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite / Sarcoidose / Sinovite / Uveíte Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite / Sarcoidose / Sinovite / Uveíte Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article