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...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Ehmer, Ursula, Lankisch, Tim O., Erichsen, Thomas J., Kalthoff, Sandra, Freiberg, Nicole, Wehmeier, Michael, Manns, Michael P., Strassburg, Christian P.
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Investigative Pathology 2008
Предметы:
Consultations in Molecular Diagnostics
Online-ссылка: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
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы