|
|
Volumn 148, Issue 5, 2014, Pages e223-e226
|
|
Familial Ebstein's anomaly, left ventricular noncompaction, and ventricular septal defect associated with an MYH7 mutation
a
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
MYOSIN HEAVY CHAIN;
MYOSIN HEAVY CHAIN 7;
UNCLASSIFIED DRUG;
CARDIAC MYOSIN;
MYH7 PROTEIN, HUMAN;
ARTICLE;
CARDIOMEGALY;
CASE REPORT;
COLOR ULTRASOUND FLOWMETRY;
EBSTEIN ANOMALY;
ECHOCARDIOGRAPHY;
FOLLOW UP;
GENE MUTATION;
GENETIC ASSOCIATION;
HEART ATRIUM SEPTUM DEFECT;
HEART VENTRICLE SEPTUM DEFECT;
HUMAN;
INFANT;
MALE;
NUCLEOTIDE SEQUENCE;
SYSTOLIC HEART MURMUR;
TRICUSPID VALVE REGURGITATION;
VENTRICULAR NONCOMPACTION;
DOPPLER ECHOCARDIOGRAPHY;
FEMALE;
GENETIC PREDISPOSITION;
GENETICS;
HEART DEFECTS, CONGENITAL;
HEART SEPTAL DEFECTS, VENTRICULAR;
HEREDITY;
MISSENSE MUTATION;
MULTIPLE MALFORMATION SYNDROME;
NEWBORN;
PEDIGREE;
PHENOTYPE;
ABNORMALITIES, MULTIPLE;
CARDIAC MYOSINS;
DNA MUTATIONAL ANALYSIS;
EBSTEIN ANOMALY;
ECHOCARDIOGRAPHY, DOPPLER, COLOR;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
HEART DEFECTS, CONGENITAL;
HEART SEPTAL DEFECTS, VENTRICULAR;
HEREDITY;
HUMANS;
INFANT, NEWBORN;
MALE;
MUTATION, MISSENSE;
MYOSIN HEAVY CHAINS;
PEDIGREE;
PHENOTYPE;
|
|
EID: 84910127803
PISSN: 00225223
EISSN: 1097685X
Source Type: Journal
DOI: 10.1016/j.jtcvs.2014.08.049 Document Type: Article |
|
Times cited : (24)
|
|
References (5)
|
