CRISPR-Cas9-mediated genome editing improves motor deficits and lifespan in a mouse model of Huntington's disease

被引：0
|
作者：
Ekman, F. K. [1 ,3 ]
Ojala, D. J. [1 ]
Adil, M. [1 ]
Lopez, P. A. [1 ]
Schaffer, D. V. [1 ]
Gaj, T. [2 ]
机构：
[1] Univ Calif Berkeley, Berkeley, CA 94720 USA
[2] Univ Illinois, Urbana, IL 61801 USA
[3] Univ Cambridge, Cambridge, England
来源：
HUMAN GENE THERAPY | 2019年 / 30卷 / 11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：
P243
引用
收藏
页码：A90 / A90
页数：1
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