Gilbert’s syndrome also called zheel-BAYR syndrome, is the most common hereditary cause of increased bilirubin. Due to genetic failure to make the enzyme UGT1A1 that breaks down the bilirubin enzyme hyperbilirubinemia occurs. GS is found in up to 5% of the population. Experteam offers a complete system for genetic analysis of Gilbert’s syndrome.
|GS.01FL||Gilbert Syndrome Kit-FL|
Capillary Electrophoresis Kit
Appl. Bios. & Beckman Coult.