Miscues on the "lack of MEF2A mutations" in coronary artery disease (multiple letters)

Journal of Clinical Investigation

Volumn 115, Issue 6, 2005, Pages 1399-1401

  Wang, Qing ^a   Rao, Shaoqi ^a   Topol, Eric J ^a   Weng, Li ^b   Cohen, Jonathan ^c   McPherson, Ruth ^d   Pennacchio, Len A ^b   Altshuler, David ^e,f,g   Hirschhorn, Joel N ^e,g,h  

^a LERNER RESEARCH INSTITUTE   (United States)

^b DOE JOINT GENOME INSTITUTE   (United States)

^c UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^d UNIVERSITY OF OTTAWA HEART INSTITUTE   (Canada)

^e HARVARD MEDICAL SCHOOL   (United States)

^f MASSACHUSETTS GENERAL HOSPITAL   (United States)

^g MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^h BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

ANGIOCARDIOGRAPHY; BRUGADA SYNDROME; CORONARY ARTERY ATHEROSCLEROSIS; CORONARY ARTERY DISEASE; DNA POLYMORPHISM; ECHOCARDIOGRAPHY; EXON; GENE; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; HEART ARRHYTHMIA; HUMAN; INTRON; LETTER; MEF2A GENE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STATISTICAL ANALYSIS; STROKE; TRANSACTIVATION; TRANSIENT ISCHEMIC ATTACK;

ADULT; AMINO ACID SUBSTITUTION; CORONARY ARTERIOSCLEROSIS; DNA-BINDING PROTEINS; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INTRONS; MADS DOMAIN PROTEINS; MALE; MIDDLE AGED; MYOGENIC REGULATORY FACTORS; POINT MUTATION; TRANSCRIPTION FACTORS;

EID: 20444444654     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI25475     Document Type: Letter

References (0)