Transcription factor HAND2 mutations in sporadic chinese patients with congenital heart disease

Chinese Medical Journal

Volumn 123, Issue 13, 2010, Pages 1623-1627

  Shen, Lei ^a   Li, Xiao Feng ^a   Shen, A Dong ^a   Wang, Qiang ^a   Liu, Cai Xia ^a   Guo, Ya Jie ^a   Song, Zhen Jiang ^a   Li, Zhong Zhi ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

BHLH; Congenital heart disease; HAND2; Mutation; Transcription factor

Indexed keywords

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR HAND2; UNCLASSIFIED DRUG;

5' UNTRANSLATED REGION; AMINO ACID SUBSTITUTION; AMINO TERMINAL SEQUENCE; ARTICLE; CHILD; CHINESE; CONGENITAL HEART DISEASE; CONTROLLED STUDY; DNA FLANKING REGION; ENDOCARDIAL CUSHION DEFECT; EXON; FEMALE; GENE AMPLIFICATION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; HEART RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION; HUMAN; INFANT; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRESCHOOL CHILD;

ASIAN CONTINENTAL ANCESTRY GROUP; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CHILD; CHILD, PRESCHOOL; GENOTYPE; HEART DEFECTS, CONGENITAL; HUMANS; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 77954471994     PISSN: 03666999     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.0366-6999.2010.13.002     Document Type: Article

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