DYSTROPHIN IMMUNOCYTOCHEMISTRY IN MUSCLE CULTURE - DETECTION OF A CARRIER OF DUCHENNE MUSCULAR-DYSTROPHY

被引：21

作者：

MIRANDA, AF

FRANCKE, U

BONILLA, E

MARTUCCI, G

SCHMIDT, B

SALVIATI, G

RUBIN, M

机构：

[1] UNIV PADUA,I-35100 PADUA,ITALY

[2] COLUMBIA UNIV,DEPT NEUROL,NEW YORK,NY 10032

[3] YALE UNIV,SCH MED,DEPT HUMAN GENET,NEW HAVEN,CT 06510

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 32卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320320231

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：268 / 273

页数：6

共 19 条

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[3] DUCHENNE MUSCULAR-DYSTROPHY - DEFICIENCY OF DYSTROPHIN AT THE MUSCLE-CELL SURFACE
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[J]. CELL, 1988, 54 (04) : 447 - 452
[4] BONILLA E, 1988, IN PRESS AM J PATHOL
[5] DIRECT METHOD FOR PRENATAL-DIAGNOSIS AND CARRIER DETECTION IN DUCHENNE BECKER MUSCULAR-DYSTROPHY USING THE ENTIRE DYSTROPHIN CDNA
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 29 (03): : 713 - 726
[6] DARRAS BT, 1988, AM J HUM GENET, V43, P620
[7] DARRAS BT, 1988, AM J HUM GENET, V43, P612
[8] PREFERENTIAL DELETION OF EXONS IN DUCHENNE AND BECKER MUSCULAR-DYSTROPHIES
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[J]. NATURE, 1987, 329 (6140) : 638 - 640
[9] DYSTROPHIN - THE PROTEIN PRODUCT OF THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS
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[J]. CELL, 1987, 51 (06) : 919 - 928
[10] COMPLETE CLONING OF THE DUCHENNE MUSCULAR-DYSTROPHY (DMD) CDNA AND PRELIMINARY GENOMIC ORGANIZATION OF THE DMD GENE IN NORMAL AND AFFECTED INDIVIDUALS
KOENIG, M
HOFFMAN, EP
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FEENER, C
KUNKEL, LM
[J]. CELL, 1987, 50 (03) : 509 - 517

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