Wilson’s disease
<p class="AbstractANGClanekAbstract"><span lang="EN-US">Wilson s disease (WD) is a genetically determined, autosomal recessive disorder of copper metabolism. The gene ATP7B encodes a copper carrier that both transports copper from hepatocyte to bile and ceruloplasmin...
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| Format: | Article |
| Language: | English |
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Slovenian Medical Association
2013-10-01
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| Series: | Zdravniški Vestnik |
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| Online Access: | http://vestnik.szd.si/index.php/ZdravVest/article/view/694 |