Alterations of lipid metabolism in Wilson disease
<p>Abstract</p> <p>Introduction</p> <p>Wilson disease (WD) is an inherited disorder of human copper metabolism, characterised by accumulation of copper predominantly in the liver and brain, leading to severe hepatic and neurological disease. Interesting findings in anim...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-05-01
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Series: | Lipids in Health and Disease |
Subjects: | |
Online Access: | http://www.lipidworld.com/content/10/1/83 |