A causative relationship between mutant IFNgR1 alleles and impaired cellular response to IFNγ in a compound heterozygous child

被引:89
作者
Altare, F
Jouanguy, E
Lamhamedi-Cherradi, S
Fondanèche, MC
Fizame, C
Ribiérre, F
Merlin, G
Dembic, Z
Schreiber, R
Lisowska-Grospierre, B
Fischer, A
Seboun, E
Casanova, JL
机构
[1] Hop Necker Enfants Malad, INSERM U429, F-75015 Paris, France
[2] Hop Necker Enfants Malad, Unite Immunol & Hematol Pediat, Paris, France
[3] Genethon, Evry, France
[4] Univ Bordeaux 2, CNRS, Unite 5016, F-33076 Bordeaux, France
[5] Inst Immunol & Rheumatol, Oslo, Norway
[6] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
关键词
D O I
10.1086/301750
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:723 / 726
页数:4
相关论文
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