Cover Image

Localization of the Wilson's disease protein in human liver

Wilson's disease is an autosomal-recessive disorder of copper metabolism that results from the absence or dysfunction of a copper-transporting P-type adenosine triphosphatase that leads to impaired biliary copper excretion and disturbed holoceruloplasmin synthesis. To gain further insight into...

Full description

Saved in:
Bibliographic Details
Main Authors: Schäfer, Mark (Author) , Roelofsen, Han (Author) , Wolters, Henk (Author) , Hofmann, Walter J. (Author) , Müller, Michael (Author) , Kuipers, Folkert (Author) , Stremmel, Wolfgang (Author) , Vonk, Roel J. (Author)
Format: Article (Journal)
Language:English
Published: 1999
In: Gastroenterology
Year: 1999, Volume: 117, Issue: 6, Pages: 1380-1385
ISSN:1528-0012
DOI:10.1016/S0016-5085(99)70288-X
Online Access:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1016/S0016-5085(99)70288-X
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S001650859970288X
Get full text
Author Notes:Mark Schaefer, Han Roelofsen, Henk Wolters, Walter J. Hofmann, Michael Müller, Folkert Kuipers, Wolfgang Stremmel, and Roel J. Vonk
Description
Summary:Wilson's disease is an autosomal-recessive disorder of copper metabolism that results from the absence or dysfunction of a copper-transporting P-type adenosine triphosphatase that leads to impaired biliary copper excretion and disturbed holoceruloplasmin synthesis. To gain further insight into the role of the Wilson's disease protein in hepatic copper handling, its localization in human liver was investigated.
Item Description:Elektronische Reproduktion der Print-Ausgabe, 28 October 2005
Gesehen am 08.06.2021
Physical Description:Online Resource
ISSN:1528-0012
DOI:10.1016/S0016-5085(99)70288-X

Similar Items