Rapid Allelic Discrimination by TaqMan PCR for the Detection of the Gilbert's Syndrome Marker UGT1A1*28

Gilbert's syndrome causes mild, unconjugated hyperbilirubinemia and is present in approximately 10% of the Caucasian population. The basis of the disorder is a 70% reduction in bilirubin glucuronidation catalyzed by the UDP-glucuronosyltransferase 1A1 (UGT1A1), which, in Caucasians, is the resu...

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Main Authors: Ehmer, Ursula, Lankisch, Tim O., Erichsen, Thomas J., Kalthoff, Sandra, Freiberg, Nicole, Wehmeier, Michael, Manns, Michael P., Strassburg, Christian P.
פורמט: Artigo
שפה:Inglês
יצא לאור: American Society for Investigative Pathology 2008
נושאים:
Consultations in Molecular Diagnostics
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC2570639/
https://ncbi.nlm.nih.gov/pubmed/18832463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2008.080036
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