Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing

• المؤلفون الرئيسيون: Radhian Amandito (مؤلف), Rinawati Rohsiswatmo (مؤلف), Erica Carolina (مؤلف), Rizka Maulida (مؤلف), Windhi Kresnawati (مؤلف), Amarila Malik (مؤلف)
• التنسيق: كتاب
• منشور في: Frontiers Media S.A., 2019-08-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Background: Single nucleotide polymorphism (SNP) variants of the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in neonatal hyperbilirubinemia (jaundice) severity. Specific ethnicities, including Asians, have certain SNPs that appear more frequ...