QuickView for UGT1A1;jsessionid=137D157AE4E16BCE090BE8A20B64C9F1;jsessionid=93D100485CC78396D38807FCC24D3889;jsessionid=C56782CA4CE0FB219933A8F26FC25A6B;jsessionid=DE131D9FBB1243B1B22868D05624F777;jsessionid=9215C1B8AFD0E8478F2EDAD75D8325AE;jsessionid=522CD04472FC13FC166479FB93091491;jsessionid=5471D4994968786195E4DDF5A4F29E9B;jsessionid=A543705A16A88353E8BD696A9AD23A8F (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=137D157AE4E16BCE090BE8A20B64C9F1;jsessionid=93D100485CC78396D38807FCC24D3889;jsessionid=C56782CA4CE0FB219933A8F26FC25A6B;jsessionid=DE131D9FBB1243B1B22868D05624F777;jsessionid=9215C1B8AFD0E8478F2EDAD75D8325AE;jsessionid=522CD04472FC13FC166479FB93091491;jsessionid=5471D4994968786195E4DDF5A4F29E9B;jsessionid=A543705A16A88353E8BD696A9AD23A8F