Drawing the line in progeria syndromes

被引:15
作者
Hegele, RA [1 ]
机构
[1] John P Robarts Res Inst, Blackburn Cardiovasc Genet Lab, London, ON N6A 5K8, Canada
关键词
D O I
10.1016/S0140-6736(03)14097-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:416 / 417
页数:2
相关论文
共 11 条
[1]  
BROWN WT, 1985, ADV EXP MED BIOL, V190, P229
[2]   Life at the edge: The nuclear envelope and human disease [J].
Burke, B ;
Stewart, CL .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (08) :575-585
[3]   LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090) [J].
Cao, HN ;
Hegele, RA .
JOURNAL OF HUMAN GENETICS, 2003, 48 (05) :271-274
[4]   Lamin A truncation in Hutchinson-Gilford progeria [J].
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 .
SCIENCE, 2003, 300 (5628) :2055-2055
[5]   Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome [J].
Eriksson, M ;
Brown, WT ;
Gordon, LB ;
Glynn, MW ;
Singer, J ;
Scott, L ;
Erdos, MR ;
Robbins, CM ;
Moses, TY ;
Berglund, P ;
Dutra, A ;
Pak, E ;
Durkin, S ;
Csoka, AB ;
Boehnke, M ;
Glover, TW ;
Collins, FS .
NATURE, 2003, 423 (6937) :293-298
[6]  
Hegele RA, 2001, CIRCULATION, V103, P2225
[7]  
IMURA H, 1985, ADV EXP MED BIOL, V190, P171
[8]   Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C [J].
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 .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (02) :426-431
[9]   Mechanisms of ageing: Public or private? [J].
Partridge, L ;
Gems, D .
NATURE REVIEWS GENETICS, 2002, 3 (03) :165-175
[10]   The nuclear lamina and inherited disease [J].
Worman, HJ ;
Courvalin, JC .
TRENDS IN CELL BIOLOGY, 2002, 12 (12) :591-598