Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference32 articles.
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3. Enhancement of glucuronide-conjugating capacity in a hyperbilirubinemic infant due to apparent enzyme induction by phenobarbital;Yaffe;New Engl. J. Med.,1966
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