Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type I
- 1 July 1992
- journal article
- research article
- Published by Wiley in The FASEB Journal
- Vol. 6 (10) , 2859-2863
- https://doi.org/10.1096/fasebj.6.10.1634050
Abstract
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