Wilson disease is an autosomal recessive disorder of copper transport and is characterized by excessive accumulation of cellular copper in the liver and other tissues because of impaired biliary copper excreti...
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Medicine by Alexandros G.Sfakianakis,Anapafseos 5 Agios Nikolaos,Crete 72100,Greece,tel :00302841026182 & 00306932607174
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Ετικέτες
Πέμπτη 15 Μαρτίου 2018
Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report
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