Lamin A truncation in Hutchinson-Gilford progeria

被引：1081

作者：

De Sandre-Giovannoli, A

Bernard, R

Cau, P

Navarro, C

Amiel, J

Boccaccio, I

Lyonnet, S

Stewart, CL

Munnich, A

Le Merrer, M

Lévy, N ^{[1
]}

机构：

[1] Fac Med Timone, INSERM, U491, Marseille, France

[2] Hop La Timone, Dept Med Genet, Marseille, France

[3] Hop Necker Enfants Malad, INSERM, U393, Paris, France

[4] Hop Conception, Biol Cellulaire Lab, Marseille, France

[5] NCI, Can & Dev Biol Lab, Frederick, MD 21702 USA

来源：

关键词：

D O I：

10.1126/science.1084125

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

[No abstract available]

引用

页码：2055 / 2055

页数：1

共 3 条

[1] Life at the edge: The nuclear envelope and human disease
Burke, B
Stewart, CL
[J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (08) : 575 - 585
[2] Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C
Novelli, G
Muchir, A
Sangiuolo, F
Helbling-Leclerc, A
D'Apice, MR
Massart, C
Capon, F
Sbraccia, P
Federici, M
Lauro, R
Tudisco, C
Pallotta, R
Scarano, G
Dallapiccola, B
Merlini, L
Bonne, G
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (02) : 426 - 431
[3] The nuclear lamina and inherited disease
Worman, HJ
Courvalin, JC
[J]. TRENDS IN CELL BIOLOGY, 2002, 12 (12) : 591 - 598