Genetic abnormalities in FOXP1 are associated with congenital heart defects

Human Mutation

Volumn 34, Issue 9, 2013, Pages 1226-1230

  Chang, Sheng Wei ^a   Mislankar, Mona ^a   Misra, Chaitali ^a   Huang, Nianyuan ^a   Dajusta, Daniel G ^c   Harrison, Steven M ^c   Mcbride, Kim L ^a,b   Baker, Linda A ^c,d   Garg, Vidu ^a,b  

^a NATIONWIDE CHILDREN S HOSPITAL   (United States)

^b OHIO STATE UNIVERSITY   (United States)

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

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

Author keywords

Atrioventricular septal defect; Cardiomyocyte; FOXP1; Hypoplastic left heart syndrome

Indexed keywords

NUCLEIC ACID BINDING PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR FOXP1; TRANSCRIPTION FACTOR NKX2.5; UNCLASSIFIED DRUG;

ARTICLE; ATRIOVENTRICULAR SEPTAL DEFECT; CARDIAC PATIENT; CELL PROLIFERATION; CHROMOSOME 3P; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; CRYPTORCHISM; EMBRYO DEVELOPMENT; ENDOCARDIAL CUSHION; EXON; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENETIC DISORDER; HAPLOINSUFFICIENCY; HEART DEVELOPMENT; HEART SINGLE VENTRICLE; HEART SURGERY; HETEROTAXY SYNDROME; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; NUCLEOTIDE SEQUENCE; PEDIATRIC SURGERY; POINT MUTATION; PRIORITY JOURNAL; PROMOTER REGION; PULMONARY VALVE ATRESIA; WESTERN BLOTTING;

EID: 84881572964     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22366     Document Type: Article

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