Mutation detection in cholestatic patients using microarray resequencing of ATP8B1 and ABCB11 [v2; ref status: indexed, http://f1000r.es/yv]

Mutation detection in cholestatic patients using microarray resequencing of ATP8B1 and ABCB11 [v2; ref status: indexed, http://f1000r.es/yv]

Background: Neonatal cholestasis is a common presentation of childhood liver diseases and can be a feature of various conditions including disorders of bile acid biogenesis and transport, various inborn errors of metabolism and perinatal infections. Some inherited metabolic diseases can be easily sc...

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Bibliographic Details
Main Authors: Kirsten E McKay, Christopher K Bruce, Jane L Hartley, A S Knisely, Ulrich Baumann, Sonja-Stephanie Bockisch, Ekkehard Sturm, Christian J Hendriksz, Deidre A Kelly, Fiona Macdonald, Paul Gissen
Format: Article
Language:English
Published: F1000 Research Ltd 2013-03-01
Series:F1000Research
Subjects:
Biliary Tract
Medical Genetics
Online Access:http://f1000research.com/articles/2-32/v2

Internet

http://f1000research.com/articles/2-32/v2

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