Functional exploration of A type lamins and associated proteins in patients affected with Hutchinson-Gilford Progeria Syndrome caused by G608G mutation in LMNA.

被引：0
|
作者：
Levy, N
Navarro, C
Boccaccio, I
Boyer, A
Negre, P
Devriendt, K
Shafeghaty, Y
Bridger, J
Philip, N
Bernard, R
Leturcq, F
Lemerrer, M
Cau, P
DeSandre-Giovannoli, A
机构：
[1] Hop Conception, Lab Biol Cellulaire, Marseille, France
[2] Hop Necker Enfants Malad, INSERM, U393, Paris, France
[3] Hop Cochin, Lab Biochim Gnt, F-75674 Paris, France
[4] Brunel Univ, Dept Biol Sci, Cell & Chromosome Biol Grp, Uxbridge UB8 3PH, Middx, England
[5] Genet Res Ctr, Tehran, Iran
[6] Ctr Memseliike Erfelijkheid Leuven, Louvain, Belgium
[7] Hop Enfants La Timone, Dept Med Genet, Marseille, France
[8] Fac Med Marseille, INSERM U491, F-13385 Marseille, France
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2263
引用
收藏
页码：554 / 554
页数：1
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