Molecular genetics of congenital atrial septal defects

Clinical Research in Cardiology

Volumn 99, Issue 3, 2010, Pages 137-147

  Posch, Maximilian G ^a,b   Perrot, Andreas ^a   Berger, Felix ^a   Özcelik, Cemil ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b DEUTSCHES HERZZENTRUM BERLIN   (Germany)

Author keywords

Atrial septal defect; Congenital heart defect; GATA4; Genetics; Mutation; NKX2.5; Sarcomeric genes; TBX20; TBX5

Indexed keywords

ACTIN; DNA; NUCLEIC ACID BINDING PROTEIN; NUCLEOTIDE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX20; TRANSCRIPTION FACTOR TBX5; UNCLASSIFIED DRUG;

ALLELE; ARM; ATRIOVENTRICULAR CONDUCTION; BLOOD FLOW; CARDIOMYOPATHY; CELL FUSION; CELL GROWTH; CELL LINEAGE; CELL MIGRATION; CELLULAR DISTRIBUTION; CHICK EMBRYO; CHINESE; CHROMOSOME; CHROMOSOME DELETION; CLINICAL FEATURE; CORONARY BLOOD VESSEL; DIGEORGE SYNDROME; DNA SEQUENCE; ENDOCARDIUM; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE EXPRESSION; GENE MAPPING; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; GENOTYPE PHENOTYPE CORRELATION; HEART; HEART ATRIUM FIBRILLATION; HEART ATRIUM SEPTUM DEFECT; HEART CONTRACTION; HEART DEVELOPMENT; HEART MUSCLE; HEART MUSCLE CELL; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HOLT ORAM SYNDROME; HOMOZYGOTE; HUMAN; IN VIVO STUDY; JAPANESE; MISSENSE MUTATION; MOLECULAR GENETICS; MORPHOGENESIS; MORTALITY; NEURAL CREST CELL; NONHUMAN; ORGANOGENESIS; PATENT FORAMEN OVALE; PHENOTYPE; PROTEIN DEGRADATION; PROTEIN EXPRESSION; RECURRENCE RISK; REVIEW; SARCOMERE; STEM CELL; STOP CODON; VELOCARDIOFACIAL SYNDROME; ZEBRA FISH;

ANIMALS; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, ATRIAL; HUMANS; INFANT, NEWBORN; MOLECULAR BIOLOGY; MUTATION; RISK FACTORS; SARCOMERES; TRANSCRIPTION FACTORS;

EID: 77950862306     PISSN: 18610684     EISSN: 18610692     Source Type: Journal    
DOI: 10.1007/s00392-009-0095-0     Document Type: Review

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