T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease

European Journal of Medical Genetics

Volumn 51, Issue 6, 2008, Pages 580-587

  Liu, Caixia ^a   Shen, Adong ^a   Li, Xiaofeng ^a   Jiao, Weiwei ^a   Zhang, Xingen ^a   Li, Zhongzhi ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

Congenital heart disease; Heart development; T box; TBX20; Transcription factor

Indexed keywords

ARTICLE; CASE REPORT; CHINESE; COMPARATIVE STUDY; CONGENITAL HEART DISEASE; EXON; FALLOT TETRALOGY; FEMALE; GENE; GENE AMPLIFICATION; GENE MUTATION; GENETIC VARIABILITY; HEART ATRIUM SEPTUM DEFECT; HUMAN; INFANT; INTRON; LUNG VEIN DRAINAGE ANOMALY; MALE; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; T BOX TRANSCRIPTION FACTOR TBX20;

CHINA; COHORT STUDIES; HEART DEFECTS, CONGENITAL; HUMANS; INTRONS; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; T-BOX DOMAIN PROTEINS;

ANIMALIA;

EID: 56649091211     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2008.09.001     Document Type: Article

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