Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy

Journal of the American College of Cardiology

Volumn 40, Issue 6, 2002, Pages 1120-1124

  Feng, Jinong ^a   Yan, Jin ^a   Buzin, Carolyn H ^a   Sommer, Steve S ^a   Towbin, Jeffrey A ^b  

^a CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATM PROTEIN; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; DYSTROPHIN; GENE PRODUCT;

ADOLESCENT; ADULT; ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; EXON; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HEART DILATATION; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PATHOGENESIS; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME LINKAGE;

ADOLESCENT; ADULT; CARDIOMYOPATHY, DILATED; CHILD; DNA MUTATIONAL ANALYSIS; DYSTROPHIN; FEMALE; HUMANS; INTRONS; LINKAGE (GENETICS); MALE; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROMOTER REGIONS (GENETICS); X CHROMOSOME;

EID: 0037130785     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0735-1097(02)02126-5     Document Type: Article

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