PEREIRA, D. L.; QURESHI, A. S. A rare case of Crigler–Najjar syndrome type II in a preterm infant: clinical, genetic and therapeutic insights into the UGT1A1 Pro176Leu variant. International Journal of Contemporary Pediatrics, [S. l.], v. 13, n. 6, p. 1018–1021, 2026. DOI: 10.18203/2349-3291.ijcp20261552. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/7313. Acesso em: 27 may. 2026.