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Gene mutations and clinical phenotypes in Chinese children with Blau syndrome.
Li, Caifeng; Zhang, Junmei; Li, Shipeng; Han, Tongxin; Kuang, Weiying; Zhou, Yifang; Deng, Jianghong; Tan, Xiaohua.
Afiliação
  • Li C; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China. caifeng_li@yeah.net.
  • Zhang J; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
  • Li S; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
  • Han T; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
  • Kuang W; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
  • Zhou Y; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
  • Deng J; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
  • Tan X; Department of Rheumatology and Immunology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
Sci China Life Sci ; 60(7): 758-762, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28639104

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite / Sinovite / Uveíte / Proteína Adaptadora de Sinalização NOD2 / Mutação Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artrite / Sinovite / Uveíte / Proteína Adaptadora de Sinalização NOD2 / Mutação Idioma: En Ano de publicação: 2017 Tipo de documento: Article