Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review-论文-万方医学网

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Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review

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第一作者： Amirifar, Parisa

作者： Amirifar, Parisa ^[1] ; Ranjouri, Mohammad Reza ^[2] ; Abolhassani, Hassan ^[3] ; Shad, Tannaz Moeini ^[4] ; Almasi-Hashiani, Amir ^[5] ; Azizi, Gholamreza ; Moamer, Soraya ; Aghamohammadi, Asghar ; Yazdani, Reza

作者单位： Univ Tehran Med Sci, Sch Med, Dept Med Genet, Tehran, Iran ^[1] Univ Tehran Med Sci, Res Ctr Immunodeficiencies, Pediat Ctr Excellence, Childrens Med Ctr, Tehran ^[2] Iran Univ Med Sci, Res Ctr Primary Immunodeficiencies, Tehran, Iran ^[3] Arak Univ Med Sci, Dept Epidemiol, Arak, Iran ^[4] Hamadan Univ Med Sci, Sch Publ Hlth, Student Res Comm, Hamadan, Hamadan, Iran ^[5]

关键词 familial hemophagocytic lymphohistiocytosis (FHL)Munc13-4 primary immunodeficiency diseases (PID)UNC13D

发布时间 2022-09-11

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Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review

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