Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation

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作者： Yoshioka,T. ^[1] ; Nishikomori,R. ^[2] ; Hara,J. ^[3] ; Okada,K. ^[4] ; Hashii,Y. ^[5] ; Okafuji,I. ; Nodomi,S. ; Kawai,T. ; Izawa,K. ; Ohnishi,H. ; Yasumi,T. ; Nakahata,T. ; Heike,T.

作者单位： Department of Pediatric Hematology and Oncology, Osaka City General Hospital, Osaka, Japan ^[1] Department of Developmental Medicine, Graduate School of Medicine, Osaka University, Suita, Japan ^[2] Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan ^[3] Department of Clinical Application, Center for IPS Cell Research and Application, Kyoto University ^[4] Department of Pediatrics, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawahara-cho ^[5]

关键词 EDA-ID HSCT IκBα NFKBIA

发布时间 2014-01-21

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Journal of Clinical Immunology

2013年33卷7期

1165-1174页

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Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation

Journal of Clinical Immunology

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Journal of Clinical Immunology

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Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation

Journal of Clinical Immunology

相似文献

Journal of Clinical Immunology

相关期刊

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