Gene mutations and clinical phenotypes in Chinese children with Blau syndrome

Science China Life Sciences

Volumn 60, Issue 7, 2017, Pages 758-762

  Li, Caifeng ^a   Zhang, Junmei ^a   Li, Shipeng ^a   Han, Tongxin ^a   Kuang, Weiying ^a   Zhou, Yifang ^a   Deng, Jianghong ^a   Tan, Xiaohua ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

Blau syndrome; clinical phenotype; genetic mutation

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; NOD2 PROTEIN, HUMAN;

ARTHRITIS; COMPLICATION; GENETICS; HUMAN; MUTATION; PHENOTYPE; SYNOVITIS; UVEITIS;

ARTHRITIS; HUMANS; MUTATION; NOD2 SIGNALING ADAPTOR PROTEIN; PHENOTYPE; SYNOVITIS; UVEITIS;

EID: 85021177280     PISSN: 16747305     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11427-017-9090-6     Document Type: Article

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