normal variations

mohammad reza heydari department of pharmacology, medical school, shiraz university of medical sciences, shiraz, iran majid fardaei department of medical genetic, medical school, shiraz university of medical sciences, shiraz, iran; department of medical genetic, medical school, shiraz university of medical sciences, zand street, postal code: 71348-53185, shiraz, iran. tel: +98-7132349610, fax: +98-7132349610 mohammad rahim kadivar department of pediatric, namazi hospital, shiraz university of medical sciences, shiraz, iran abbas rezaianzadeh department of epidemiology, shiraz university of medical sciences, shiraz, iran mohammad reza panjehshahin department of pharmacology, medical school, shiraz university of medical sciences, shiraz, iran zeinab gholami bardeji department of radiology, medical imaging research center, namazi hospital, shiraz university of medical sciences, shiraz, iran

conclusions the present findings showed that the ta7/7 promoter of ugt1a1 gene accounted for a considerable number of gilbert’s syndrome cases (11.3%). the studied variations had a significant effect on creatine phosphokinase and serum total bilirubin levels. results about 78.9% of the studied subjects had normal homozygous genotypes, and 21.1% were heterozygous for the gly71arg variation. in t...

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