Inherited metabolic disease.

Abstract:

:The elucidation of metabolic pathways and the genetic basis for diseases of the liver continues to increase our understanding of disease pathogenesis and advance treatment options. This selective review covers a wide range of subjects, from the identification of novel proteins and the importance of specific transport pathways to phenotypic expression of disease and management of acute liver failure. Three selected disorders--Wilson disease, genetic hemochromatosis and other hereditary iron overload disorders, and alpha(1)-antitrypsin disease--are the focus of this review.

authors

Schilsky ML

doi

10.1097/00001574-200205000-00003

subject

Has Abstract

pub_date

2002-05-01 00:00:00

pages

299-306

issue

3

eissn

0267-1379

issn

1531-7056

pii

00001574-200205000-00003

journal_volume

18

pub_type

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