GI highlights from the literature

Wilson's disease (WD) is an autosomal recessive disorder, which develops due to gene mutations in the copper transporter ATPase copper-transporting [beta] (Atp7b), impairing copper excretion into bile and resulting in copper accumulation in the liver. [...]novel medical therapies for this cohor...

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Veröffentlicht in:	Gut 2016-10, Vol.65 (10), p.1777-1778
1. Verfasser:	McLean, Mairi H
Format:	Artikel
Sprache:	eng
Schlagworte:	Cancer Copper Gastroenterology Hepatology Homeostasis Hydrocarbons Inflammatory bowel disease Liver diseases Metabolism Mutation Rodents Studies Transplants & implants Tumors Vitamin D
Online-Zugang:	Volltext
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