Title : UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.

Pub. Date : 2013 Nov

PMID : 23992562






1 Functional Relationships(s)
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Organism
1 Differential diagnosis of CN1 and CN2 was made on the basis of patient"s response to phenobarbitone. Phenobarbital 5'-nucleotidase, cytosolic IA Homo sapiens