Mutation Analysis of the ATP7B Gene in Seven Chinese Families with Wilson’s Disease

Background: Wilson’s disease (WD) is an autosomal recessive disease, which is characterized by an excessive copper accumulation in the liver and brain, leading to subsequent hepatic and/or neurological disorders. The causative gene for WD has been identified as the ATPase Cu 2+ transporting beta pol...

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Veröffentlicht in:	Digestion 2019-01, Vol.99 (4), p.319-326
Hauptverfasser:	Xiao, Heng, Deng, Sheng, Deng, Xiong, Gu, Shaojuan, Yang, Zhijian, Yin, Hang, Deng, Hao
Format:	Artikel
Sprache:	eng
Schlagworte:	Original Paper
Online-Zugang:	Volltext
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