Title : [Clinical features and gene mutation profiles of patients with chronic hepatitis B and Gilbert's syndrome].

Pub. Date : 2015 Jan

PMID : 25751380






1 Functional Relationships(s)
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1 RESULTS: Sequencing of the Gilbert syndrome-associated gene, UGT 1A 1, revealed mutations in the upstream promoter phenobarbital-responsive element module (PBREM) (-3279 mutation, 23 cases), in the promoter TATA box (a TA insertion mutation, 21 cases), and in the coding region of exon 1 (a GGA-AGA Gly71Arg mutation, 18 cases); there was no statistical difference found for any of the three mutations among this patient population (x2 =1.640, P more than 0.05). Phenobarbital UDP glucuronosyltransferase family 1 member A1 Homo sapiens