Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects

Published 2015 View Full Article

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Journal

MEDICINE

Volume 94, Issue 22, Pages e925

Publisher

Ovid Technologies (Wolters Kluwer Health)

Online

2015-06-03

DOI

10.1097/md.0000000000000925

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