Identification of Two Novel Genetic Alterations as Possible Causes of Combined Immunodeficiency

被引：0
|
作者：
Fuehrer, M. [1 ]
Pannicke, U. [1 ]
Hoenig, M. [2 ]
Baumann, B. [3 ]
Enders, A. [4 ]
Enders, A. [4 ]
Holzmann, K. [5 ]
Schuetz, C. [2 ]
Friedrich, W. [2 ]
Schulz, A. [2 ]
Schwarz, K. [6 ]
机构：
[1] Univ Ulm, Inst Transfus Med, D-89069 Ulm, Germany
[2] Univ Med Ctr Ulm, Dept Pediat, Ulm, Germany
[3] Univ Ulm, Inst Physiol Chem, D-89069 Ulm, Germany
[4] Australian Natl Univ, John Curtin Sch Med Res, Dept Immunol, Canberra, ACT 2601, Australia
[5] Univ Ulm, Genom Core Facil, D-89069 Ulm, Germany
[6] German Red Cross Blood Serv Baden Wurttemberg Hes, Inst Clin Transfus Med & Immunogenet, Ulm, Germany
来源：
JOURNAL OF CLINICAL IMMUNOLOGY | 2014年 / 34卷
关键词：
D O I：
暂无
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
ESID-0319
引用
收藏
页码：S384 / S384
页数：1
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