Wang, Lejin <br/><br/>
Mutation of MEF2A in an inherited disorder with features of coronary artery disease.  [electronic resource] 

 -  Science (New York, N.Y.)  Nov 2003 
 - 1578-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1095-9203 
<br/><br/><label>Standard No.: </label>10.1126/science.1088477  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Amino Acid Sequence<br/>Animals<br/>Arteries--metabolism<br/>Base Sequence<br/>Cell Nucleus--metabolism<br/>Chromosomes, Human, Pair 15--genetics<br/>Coronary Artery Disease--genetics<br/>Coronary Vessels--metabolism<br/>DNA-Binding Proteins--chemistry<br/>Dimerization<br/>Endothelium, Vascular--metabolism<br/>Erythroid-Specific DNA-Binding Factors<br/>Female<br/>Fluorescent Antibody Technique<br/>GATA1 Transcription Factor<br/>Gene Expression<br/>Genes, Dominant<br/>Genetic Linkage<br/>Genetic Markers<br/>Genetic Predisposition to Disease<br/>Humans<br/>MADS Domain Proteins<br/>MEF2 Transcription Factors<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Muscle, Smooth--cytology<br/>Myocardial Infarction--genetics<br/>Myogenic Regulatory Factors<br/>Pedigree<br/>Protein Binding<br/>Protein Conformation<br/>Protein Structure, Tertiary<br/>Protein Transport<br/>Rats<br/>Risk Factors<br/>Sequence Deletion<br/>Signal Transduction<br/>Transcription Factors--chemistry<br/>Transcriptional Activation