Literature DB >> 8276413

Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2.

N Moghrabi1, D J Clarke, M Boxer, B Burchell.   

Abstract

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Year:  1993        PMID: 8276413     DOI: 10.1006/geno.1993.1451

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


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  18 in total

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9.  Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.

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