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dc.creatorArrese J.,Marco
dc.date1999-09-01
dc.date.accessioned2019-09-10T12:38:48Z
dc.date.available2019-09-10T12:38:48Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0034-98871999000900013
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/104810
dc.descriptionRecent molecular studies have resulted in the identification of genetic alterations underlying several hereditary disorders of the liver. Cloning of disease genes are increasing our understanding of the basic defects in liver diseases. This review focuses on selected inherited liver diseases such as hyperbilirubinemic syndromes, hemochromatosis, Wilson disease and genetic cholestatic syndromes and illustrate the knowledge gained on these disorders from molecular studies. Potential implications of the identification of disease genes such as practical applications for diagnosis, information on prognosis and the possibility to design new therapies are discussed.
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dc.languagees
dc.publisherSociedad Médica de Santiago
dc.relation10.4067/S0034-98871999000900013
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceRevista médica de Chile v.127 n.9 1999
dc.subjectEpidemiology molecular
dc.subjectGenetics, biochemical
dc.subjectMolecular biology
dc.subjectMolecular medicine
dc.titleIdentificación de defectos moleculares en las enfermedades hepáticas.: Ejemplos recientes


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