Diagnosis of gilbert's syndrome via pyrosequencing in clinical practice

Relevance. Gilbert's syndrome (GS) is a disease with an autosomal recessive type of inheritance caused by either impaired expression of the UGT1A1 gene, which encodes the isoform of the uridine-5-diphosphate glucuronosyltransferase (UDP-GTA1), or structural modifications of UDP-GTA1. GS is char...

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Main Authors: L. I. Melnikova (Author), L. Yu. Ilchenko (Author), E. A. Dunaeva (Author), M. V. Kozitsyna (Author), O. P. Dribnokhodova (Author), K. O. Mironov (Author)
Format: Book
Published: SINAPS LLC, 2019-11-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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