No association between the Friedreich's ataxia gene and NIDDM in the French population

被引:11
作者
Dupont, S
Dubois, D
Vionnet, N
Boitard, C
Caillat-Zucman, S
Timsit, J
Froguel, P
机构
[1] Inst Pasteur, CNRS, EP10, F-59019 Lille, France
[2] Hop Necker Enfants Malad, Serv Immunol Clin, Paris, France
[3] Hop Necker Enfants Malad, Unite Diabetol, Paris, France
关键词
D O I
10.2337/diabetes.47.10.1654
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:1654 / 1656
页数:3
相关论文
共 14 条
[11]   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
[12]  
*SAGE, 1994, SAGE STAT AN GEN EP
[13]   COMPARISON OF FLUORESCENCE-BASED SEMIAUTOMATED GENOTYPING OF MULTIPLE MICROSATELLITE LOCI WITH AUTORADIOGRAPHIC TECHNIQUES [J].
SCHWENGEL, DA ;
JEDLICKA, AE ;
NANTHAKUMAR, EJ ;
WEBER, JL ;
LEVITT, RC .
GENOMICS, 1994, 22 (01) :46-54
[14]   Genetics of NIDDM in France - Studies with 19 candidate genes in affected sib pairs [J].
Vionnet, N ;
Hani, EH ;
Lesage, S ;
Philippi, A ;
Hager, J ;
Varret, M ;
Stoffel, M ;
Tanizawa, Y ;
Chiu, KC ;
Glaser, B ;
Permutt, MA ;
Passa, P ;
Demenais, F ;
Froguel, P .
DIABETES, 1997, 46 (06) :1062-1068