Contribution of the TATA-Box Genotype (Gilbert Syndrome) to Serum Bilirubin Concentrations in the Italian Population
Author:
Affiliation:
1. Laboratorio di Chimica Clinica e Microbiologia, Azienda Ospedaliera San Paolo, Via di Rudinı̀ 8, 20142 Milan, Italy;
2. Clinica Pediatrica, Azienda Ospedaliera San Paolo, Università di Milano, Via di Rudinı̀ 8, 20142 Milan, Italy
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/45/6/897/32721377/clinchem0897.pdf
Reference10 articles.
1. Pathogenesis of Gilbert's syndrome
2. Gilbert's syndrome
3. Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome
4. The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome
5. A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini.
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