Nuclear power and mitochondrial disease

被引:51
作者
DiMauro, S
Schon, EA
机构
[1] Columbia Univ Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
关键词
D O I
10.1038/883
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:214 / 215
页数:2
相关论文
共 12 条
[1]   MUTATION OF A NUCLEAR SUCCINATE-DEHYDROGENASE GENE RESULTS IN MITOCHONDRIAL RESPIRATORY-CHAIN DEFICIENCY [J].
BOURGERON, T ;
RUSTIN, P ;
CHRETIEN, D ;
BIRCHMACHIN, M ;
BOURGEOIS, M ;
VIEGASPEQUIGNOT, E ;
MUNNICH, A ;
ROTIG, A .
NATURE GENETICS, 1995, 11 (02) :144-149
[2]  
CANDERHEUVEL L, 1998, AM J HUM GENET, V62, P262
[3]   Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease [J].
Casari, G ;
De Fusco, M ;
Ciarmatori, S ;
Zeviani, M ;
Mora, M ;
Fernandez, P ;
De Michele, G ;
Filla, A ;
Cocozza, S ;
Marconi, R ;
Dürr, A ;
Fontaine, B ;
Ballabio, A .
CELL, 1998, 93 (06) :973-983
[4]   Mitochondrial DNA and diseases of the nervous system: The spectrum [J].
DiMauro, S ;
Schon, EA .
NEUROSCIENTIST, 1998, 4 (01) :53-63
[5]   Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin [J].
Koutnikova, H ;
Campuzano, V ;
Foury, F ;
Dolle, P ;
Cazzalini, O ;
Koenig, M .
NATURE GENETICS, 1997, 16 (04) :345-351
[6]   Molecular genetic aspects of human mitochondrial disorders [J].
Larsson, NG ;
Clayton, DA .
ANNUAL REVIEW OF GENETICS, 1995, 29 :151-178
[7]   THE DEVELOPMENT OF MITOCHONDRIAL MEDICINE [J].
LUFT, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8731-8738
[8]   Localization of the Wilson's disease protein product to mitochondria [J].
Lutsenko, S ;
Cooper, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6004-6009
[9]  
MORAES CT, 1993, J CLIN INVEST, V92, P2906, DOI 10.1172/JCI116913
[10]   Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia [J].
Rotig, A ;
deLonlay, P ;
Chretien, D ;
Foury, F ;
Koenig, M ;
Sidi, D ;
Munnich, A ;
Rustin, P .
NATURE GENETICS, 1997, 17 (02) :215-217