Mocanu, N.; Sacară, V.; Groppa, St.
(Ministerul Sănătăţii al Republicii Moldova, Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, 2011)
Wilson’s disease (WD) is an autosomal recessive disorder of copper transport caused by a defect in the ATP7B gene. The disorder manifests as chronic liver disease and/or neurological impairment due to accumulation of copper ...