Development of T cell mediated gene therapy for correction of humoral and cytotoxic defects in X-linked lymphoproliferative disease (XLP)

被引：0
|
作者：
Panchal, Neelam [1 ]
Houghton, Benjamin [1 ]
Diez, Begona [1 ]
Thrasher, Adrian [1 ,2 ]
Gaspar, Bobby [1 ,2 ]
Booth, Claire [1 ,2 ]
机构：
[1] UCL GOSH Inst Child Hlth, Mol & Cellular Immunol Sect, London, England
[2] Great Ormond St Hosp Sick Children, Dept Paediat Immunol, London, England
来源：
HUMAN GENE THERAPY | 2017年 / 28卷 / 08期
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D O I：
暂无
中图分类号：
Q81 [生物工程学（生物技术）]; Q93 [微生物学];
学科分类号：
071005 ; 0836 ; 090102 ; 100705 ;
摘要：
FB02
引用
收藏
页码：A10 / A11
页数：2
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