Mutations of ZFPM2/FOG2 Gene in Sporadic Cases of Tetralogy of Fallot

Human Mutation

Volumn 22, Issue 5, 2003, Pages 372-377

  Pizzuti, Antonio ^a,b   Sarkozy, Anna ^a,b   Newton, Anthea L ^e   Conti, Emanuela ^b   Flex, Elisabetta ^a,b   Digilio, Maria Cristina ^c   Amati, Francesca ^d   Gianni, Debora ^a,b   Tandoi, Caterina ^a,b   Marino, Bruno ^a   Crossley, Merlin ^e   Dallapiccola, Bruno ^a,b  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^c BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^d UNIVERSITY OF ROME TOR VERGATA   (Italy)

^e Istituto CSS Mendel ^*

Author keywords

Conotruncal heart defect; CTD; FOG2; GATA4; Tetralogy of Fallot; TOF; ZFPM2

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; DNA; PROTEIN; TRANSCRIPTION FACTOR GATA 4;

ADOLESCENT; AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; ECHOCARDIOGRAPHY; FALLOT TETRALOGY; FEMALE; GENE; GENE ACTIVATION; GENE MUTATION; GENE SEQUENCE; HUMAN; INFANT; MALE; MISSENSE MUTATION; MOUSE; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN INTERACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; THORAX RADIOGRAPHY;

ADOLESCENT; ANIMALS; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA-BINDING PROTEINS; HUMANS; INFANT; INFANT, NEWBORN; MICE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NIH 3T3 CELLS; TETRALOGY OF FALLOT; TRANSCRIPTION FACTORS;

EID: 10744226877     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10261     Document Type: Article

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