MORE DELETIONS IN THE 5' REGION THAN IN THE CENTRAL REGION OF THE DYSTROPHIN GENE WERE IDENTIFIED AMONG FILIPINO DUCHENNE AND BECKER MUSCULAR-DYSTROPHY PATIENTS

被引:5
作者
CUTIONGCO, EM
PADILLA, CD
TAKENAKA, K
YAMASAKI, Y
MATSUO, M
NISHIO, H
机构
[1] KOBE UNIV,SCH MED,INT CTR MED RES,DIV GENET,KOBE 650,JAPAN
[2] KOBE UNIV,SCH MED,DEPT PEDIAT,KOBE 650,JAPAN
[3] UNIV PHILIPPINES,PHILIPPINE GEN HOSP,COLL MED,DEPT PEDIAT,MANILA,PHILIPPINES
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 59卷 / 02期
关键词
D O I
10.1002/ajmg.1320590228
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:266 / 267
页数:2
相关论文
共 13 条
[1]   MOLECULAR AND CLINICAL CORRELATIONS OF DELETIONS LEADING TO DUCHENNE AND BECKER MUSCULAR-DYSTROPHIES [J].
BAUMBACH, LL ;
CHAMBERLAIN, JS ;
WARD, PA ;
FARWELL, NJ ;
CASKEY, CT .
NEUROLOGY, 1989, 39 (04) :465-474
[2]  
BEGGS AH, 1990, HUM GENET, V86, P45
[3]   242 BREAKPOINTS IN THE 200-KB DELETION-PRONE P20-REGION OF THE DMD GENE ARE WIDELY SPREAD [J].
BLONDEN, LAJ ;
GROOTSCHOLTEN, PM ;
DENDUNNEN, JT ;
BAKKER, E ;
ABBS, S ;
BOBROW, M ;
BOEHM, C ;
VAN BROECKHOVEN, C ;
BAUMBACH, L ;
CHAMBERLAIN, J ;
CASKEY, CT ;
DENTON, M ;
FELICETTI, L ;
GALLUZI, G ;
FISCHBECK, KH ;
FRANCKE, U ;
DARRAS, B ;
GILGENKRANTZ, H ;
KAPLAN, JC ;
HERRMANN, FH ;
JUNIEN, C ;
BOILEAU, C ;
LIECHTIGALLATI, S ;
LINDLOF, M ;
MATSUMOTO, T ;
NIIKAWA, N ;
MULLER, CR ;
PONCIN, J ;
MALCOLM, S ;
ROBERTSON, E ;
ROMEO, G ;
COVONE, AE ;
SCHEFFER, H ;
SCHRODER, E ;
SCHWARTZ, M ;
VERELLEN, C ;
WALKER, A ;
WORTON, R ;
GILLARD, E ;
VANOMMEN, GJB .
GENOMICS, 1991, 10 (03) :631-639
[4]  
FORREST S M, 1988, Genomics, V2, P109, DOI 10.1016/0888-7543(88)90091-2
[5]   AMPLIFICATION OF 10 DELETION-RICH EXONS OF THE DYSTROPHIN GENE BY POLYMERASE CHAIN-REACTION SHOWS DELETIONS IN 36 OF 90 JAPANESE FAMILIES WITH DUCHENNE MUSCULAR-DYSTROPHY [J].
KITOH, Y ;
MATSUO, M ;
NISHIO, H ;
TAKUMI, T ;
NAKAJIMA, T ;
MASUMURA, T ;
KOGA, J ;
NAKAMURA, H .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 42 (04) :453-457
[6]  
KOENIG M, 1989, AM J HUM GENET, V45, P498
[7]   COMPLETE CLONING OF THE DUCHENNE MUSCULAR-DYSTROPHY (DMD) CDNA AND PRELIMINARY GENOMIC ORGANIZATION OF THE DMD GENE IN NORMAL AND AFFECTED INDIVIDUALS [J].
KOENIG, M ;
HOFFMAN, EP ;
BERTELSON, CJ ;
MONACO, AP ;
FEENER, C ;
KUNKEL, LM .
CELL, 1987, 50 (03) :509-517
[8]  
LAU YL, 1992, CLIN GENET, V41, P252
[9]   A VERY SMALL FRAME-SHIFTING DELETION WITHIN EXON-19 OF THE DUCHENNE MUSCULAR-DYSTROPHY GENE [J].
MATSUO, M ;
MASUMURA, T ;
NAKAJIMA, T ;
KITOH, Y ;
TAKUMI, T ;
NISHIO, H ;
KOGA, J ;
NAKAMURA, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (02) :963-967
[10]   2 HOT-SPOTS OF RECOMBINATION IN THE DMD GENE CORRELATE WITH THE DELETION PRONE REGIONS [J].
OUDET, C ;
HANAUER, A ;
CLEMENS, P ;
CASKEY, T ;
MANDEL, JL .
HUMAN MOLECULAR GENETICS, 1992, 1 (08) :599-603