Lentiviral vectors-mediated gene transfer as a new strategy to model Huntington's disease

被引：0
|
作者：
Déglon, N
de Almeida, LP
Palfi, S
Régulier, E
Bloch, J
Condé, F
Brouillet, E
Aebischer, P
Hantraye, P
机构：
[1] Swiss Fed Inst Technol, Inst Neurosci, CH-1015 Lausanne, Switzerland
[2] Univ Lausanne, Sch Med, Lausanne, Switzerland
[3] Univ Coimbra, Fac Pharm, Pharm Tech Lab, P-3000 Coimbra, Portugal
[4] Univ Coimbra, Ctr Neurosci, P-3000 Coimbra, Portugal
[5] CEA, Serv Hosp Frederic Joliot, CNRS, URA 2210, F-91406 Orsay, France
来源：
CELL TRANSPLANTATION | 2003年 / 12卷 / 03期
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中图分类号：
Q813 [细胞工程];
学科分类号：
摘要：
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页码：318 / 318
页数：1
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