Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy
Božina, N., Šušak Sporiš, I., Klarica Domjanović, I., Ganoci, L., Šimičević, L., Lovrić, M. ... Trkulja, V. (2023). Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy. European Journal of Clinical Pharmacology, 79. (8), 1117-1129. doi: 10.1007/s00228-023-03526-z
Božina, Nada, et al. "Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy." European Journal of Clinical Pharmacology, vol. 79, br. 8, 2023, str. 1117-1129. https://doi.org/10.1007/s00228-023-03526-z
Božina, Nada, Ivana Šušak Sporiš, Iva Klarica Domjanović, Lana Ganoci, Livija Šimičević, Mila Lovrić, Zrinka Čolak Romić, Željka Petelin Gadže i Vladimir Trkulja. "Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy." European Journal of Clinical Pharmacology 79, br. 8 (2023): 1117-1129. https://doi.org/10.1007/s00228-023-03526-z
Božina, N., et al. (2023) 'Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy', European Journal of Clinical Pharmacology, 79(8), str. 1117-1129. doi: 10.1007/s00228-023-03526-z
Božina N, Šušak Sporiš I, Klarica Domjanović I, Ganoci L, Šimičević L, Lovrić M, i sur.. Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy. European Journal of Clinical Pharmacology [Internet]. 08.2023. [pristupljeno 05.10.2024.];79(8):1117-1129. doi: 10.1007/s00228-023-03526-z
N. Božina, et al., "Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy", European Journal of Clinical Pharmacology, vol. 79, br. 8, str. 1117-1129, Kolovoz 2023. [Online]. Dostupno na: https://urn.nsk.hr/urn:nbn:hr:105:062920. [Citirano: 05.10.2024.]