ALDH1A2 (RALDH2) genetic variation in human congenital heart disease

BMC Medical Genetics

Volumn 10, Issue , 2009, Pages 113-

  Pavan, Marilene ^a   Ruiz, Viviane F ^a   Silva, Fábio A ^a   Sobreira, Tiago J ^a   Cravo, Roberta M ^a   Vasconcelos, Michelle ^a   Marques, Lívia P ^a   Mesquita, Sonia M F ^a   Krieger, José E ^a   Lopes, Antônio A B ^a   Oliveira, Paulo S ^a   Pereira, Alexandre C ^a   Xavier Neto, José ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

RETINAL DEHYDROGENASE; RETINAL DEHYDROGENASE TYPE II; UNCLASSIFIED DRUG;

ARTICLE; CONGENITAL HEART DISEASE; ENZYME ACTIVITY; EXON; FALLOT TETRALOGY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MOLECULAR DYNAMICS; NUCLEOTIDE SEQUENCE; OLIGOMERIZATION; PHYLOGENETIC TREE; POLYMERASE CHAIN REACTION; PROTEIN DOMAIN; PROTEIN MOTIF; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ALIGNMENT; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM; TRANSCRIPTION INITIATION SITE;

SANDER;

CELL LINE; CHROMOSOMES, HUMAN, PAIR 15; EXONS; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HEART DEFECTS, CONGENITAL; HUMANS; LINKAGE DISEQUILIBRIUM; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN FOLDING; RETINAL DEHYDROGENASE; TETRALOGY OF FALLOT;

EID: 70749153565     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-10-113     Document Type: Article

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