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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Αλέξανδρος Γ. Σφακιανάκης
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5
Άγιος Νικόλαος Κρήτη 72100
2841026182
6032607174
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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