TY - CHAP M1 - Book, Section TI - Wilson’s Disease A1 - Brewer, George J. A2 - Kasper, Dennis A2 - Fauci, Anthony A2 - Hauser, Stephen A2 - Longo, Dan A2 - Jameson, J. Larry A2 - Loscalzo, Joseph PY - 2014 T2 - Harrison's Principles of Internal Medicine, 19e AB - Wilson’s disease is an autosomal recessive disorder caused by mutations in the ATP7B gene, which encodes a membrane-bound, copper-transporting ATPase. Clinical manifestations are caused by copper toxicity and primarily involve the liver and the brain. Because effective treatment is available, it is important to make this diagnosis early. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2021/03/05 UR - accesspharmacy.mhmedical.com/content.aspx?aid=1120817430 ER -