QuickView for UGT1A1;jsessionid=C669C989F11B99FE2268F11C8C1B0FD0 (gene)

1. A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndr…
2. Dutch pharmacogenetics working group (DPWG) guideline for the gene-drug interaction between UGT1A1 a…
3. TaqMan real time PCR for the Detection of the Gilbert's Syndrome Markers UGT1A1*28; UGT1A1*36 and UG…
4. Epigenetics and microRNAs in UGT1As.
5. Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patient…

There were no clinical trials for UGT1A1;jsessionid=C669C989F11B99FE2268F11C8C1B0FD0