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10.1038/emboj.2013.74 EMBO J
L., Moisand C., Chalon P., et al
The underlying cause of this disorder is a polymorphism in the promoter region of the UGT isoform 1A1 gene ( UGT1A1*28 ) that increases the length of the promoter [97]
The principle of lowest effective dose for the shortest duration remains essential
Vitamin B Supplementation: What's the Right Choice for Your Patients
M.DenisC
