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) |
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Format: | Book |
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SINAPS LLC,
2019-11-01T00:00:00Z.
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