reference/6907532

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endingPage	2863
issn	0892-6638 1530-6860
issueIdentifier	10
pageRange	2859-2863
publicationName	FASEB journal : official publication of the Federation of American Societies for Experimental Biology
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bibliographicCitation	Bosma PJ, Chowdhury JR, Huang TJ, Lahiri P, Elferink RP, Van Es HH, Lederstein M, Whitington PF, Jansen PL, Chowdhury NR. Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type I. FASEB J. 1992 Jul;6(10):2859–63. doi: 10.1096/fasebj.6.10.1634050. PMID: 1634050.
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date	199207
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type I
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