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Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene

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Bibliographic Details
Published in:	Journal of medical genetics 2000-09, Vol.37 (9), p.712-713
Main Authors:	IOLASCON, ACHILLE, MELONI, ALESSANDRA, COPPOLA, BRIGIDA, ROSATELLI, MARIA CRISTINA
Format:	Article
Language:	English
Subjects:	Adolescent Amino Acid Substitution Bilirubin - blood Crigler-Najjar Syndrome - enzymology Crigler-Najjar Syndrome - genetics Crigler-Najjar Syndrome - pathology DNA - chemistry DNA - genetics DNA Mutational Analysis Family Health Female Glucuronosyltransferase - genetics Humans Letters to the Editor Male Mutation Point Mutation Polymorphism, Genetic Promoter Regions, Genetic Sequence Deletion
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