Fig. 1
From: A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report
Sequencing chromatograms of the patient and her parents. The row in each chromatograms indicated the position of the identified mutation. a The sequence of normal bases in this specific part of the UGT1A1 gene was shown in the upper row, whereas the matched lower row showed the bases (CAT) that were inserted in the patient (a1) and her mother (a2). b The sequence of normal bases in this specific of the UGT1A1 gene is shown in the upper row, whereas the matched lower row showed the deleted bases (AA) in the patient (b1) and her father (b2)