Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome.
第一作者:
D,Pirulli
第一单位:
Servizio di Genetica Medica, Instituto di Ricovero e Cura a Carattere Scientifico Burlo Garofolo and Università di Trieste, 34137 Trieste, Italy.
作者:
医学主题词
青少年(Adolescent);成年人(Adult);色谱法, 高压液相(Chromatography, High Pressure Liquid);女(雌)性(Female);吉尔伯特病(Gilbert Disease);葡糖醛酸基转移酶(Glucuronosyltransferase);人类(Humans);男(雄)性(Male);聚合酶链反应(Polymerase Chain Reaction);多态现象, 遗传(Polymorphism, Genetic);启动区, 遗传(Promoter Regions, Genetic)
PMID
10620585
发布时间
2019-07-22
- 浏览7
Clinical chemistry
129-31页
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