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Different clinical phenotypes in 2 siblings with X-linked severe combined immunodeficiency
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نویسنده
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wada t. ,toma t. ,yasui m. ,inoue m. ,kawa k. ,imai k. ,morio t. ,yachie a.
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منبع
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journal of investigational allergology and clinical immunology - 2016 - دوره : 26 - شماره : 1 - صفحه:63 -65
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چکیده
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[no abstract available]
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کلیدواژه
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Common γ chain; Leaky phenotype; Omenn syndrome; Severe combined immunodeficiency; T cells
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آدرس
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department of pediatrics,school of medicine,institute of medical,pharmaceutical and health sciences,kanazawa university,kanazawa, Japan, department of pediatrics,school of medicine,institute of medical,pharmaceutical and health sciences,kanazawa university,kanazawa, Japan, department of hematology/oncology,osaka medical center and research institute for maternal and child health,osaka, Japan, department of hematology/oncology,osaka medical center and research institute for maternal and child health,osaka, Japan, department of hematology/oncology,osaka medical center and research institute for maternal and child health,osaka, Japan, department of pediatrics,tokyo medical and dental university,tokyo, Japan, department of pediatrics,tokyo medical and dental university,tokyo, Japan, department of pediatrics,school of medicine,institute of medical,pharmaceutical and health sciences,kanazawa university,kanazawa, Japan
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Authors
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