Gilbert syndrome: Analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population

European Journal of Pediatrics

Volumn 159, Issue 11, 2000, Pages 873-874

  Kavazarakis, Emmanuel ^a   Tsezou, Aspasia ^a   Tzetis, Maria ^a   Hadjidimoula, Androniki ^a   Kitsiou, Sofia ^a   Kanavakis, Emmanuel ^a   Karpathios, Themistocles ^a  

^a UNIVERSITY OF ATHENS   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCURONOSYLTRANSFERASE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; FEMALE; GENETIC ANALYSIS; GENOTYPE; GILBERT DISEASE; GREECE; HUMAN; MAJOR CLINICAL STUDY; MALE; POPULATION GENETICS; POPULATION RESEARCH; PRIORITY JOURNAL; PROMOTER REGION;

EID: 0033771417     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310000603     Document Type: Article

References (6)

1. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase in Gilbert syndrome
2. UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis
3. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert syndrome
4. Population studies on Gilbert syndrome
5. The novel bilirubin/phenol UDP-glucuronosyltransferase UGT1 gene locus: Implications for multiple nonhemolytic familial hyperbilirubinemia phenotypes
6. A novel complex locus UGT1 encodes human bilirubin phenol and other UDP-glucuronosyltransferase isoenzymes with identical carboxyl termini