Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects

Cardiology in the Young

Volumn 19, Issue 5, 2009, Pages 482-485

  Hamanoue, Haruka ^a   Rahayuningsih, Sri Endah ^b   Hirahara, Yuya ^a   Itoh, Junko ^a   Yokoyama, Utako ^a   Mizuguchi, Takeshi ^a   Saitsu, Hirotomo ^a   Miyake, Noriko ^a   Hirahara, Fumiki ^a   Matsumoto, Naomichi ^a  

^a YOKOHAMA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b PADJADJARAN UNIVERSITY   (Indonesia)

Author keywords

Genetic inheritance; Interatrial communications; New mutation

Indexed keywords

TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; GATA4 PROTEIN, HUMAN;

ARTICLE; CHILD; CONTROLLED STUDY; FALLOT TETRALOGY; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC SCREENING; HEART ATRIUM SEPTUM DEFECT; HUMAN; MAJOR CLINICAL STUDY; PRESCHOOL CHILD; GENETICS; HEART SEPTUM DEFECT; MALE; MUTATION; PEDIGREE;

CHILD, PRESCHOOL; GATA4 TRANSCRIPTION FACTOR; GENETIC TESTING; HEART SEPTAL DEFECTS, ATRIAL; HUMANS; MALE; MUTATION; PEDIGREE; TETRALOGY OF FALLOT;

EID: 75549089626     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951109990813     Document Type: Article

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