Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of fallot

Journal of International Medical Research

Volumn 35, Issue 6, 2007, Pages 867-872

  Erdal, Esra ^a   Erdal, C ^a   Bulut, G ^a   Kunter, I ^a   Kir, M ^a   Atabey, N ^a   Açikel, Ü ^a  

^a DOKUZ EYLUL UNIVERSITY   (Turkey)

Author keywords

Mutation analysis; Tetralogy of Fallot; Vangl2 gene

Indexed keywords

MEMBRANE PROTEIN; UNCLASSIFIED DRUG; VANGL2 PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; CONTROLLED STUDY; EXON; FALLOT TETRALOGY; GENETIC POLYMORPHISM; HUMAN; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRESCHOOL CHILD;

EID: 36949024028     PISSN: 03000605     EISSN: None     Source Type: Journal    
DOI: 10.1177/147323000703500614     Document Type: Article

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