The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

R.E. Tanzi (1) , K. Petrukhin (2) , I. Chernov (2) , J.L. Pellequer (2) , W. Wasco (1) , B. Ross (2) , D.M. Romano (1) , E. Parano (3) , L. Pavone (3) , L.M. Brzustowicz (2) , M. Devoto (2) , J. Peppercorn (1) , A.I. Bush (1) , I. Sternlieb (2, 4) , M. Pirastu , J.F. Gusella (1) , O. Evgrafov , G.K. Penchaszadeh (2) , B. Honig (2) , I.S. Edelman (2) , M.B. Soares (2) , I.H. Scheinberg (2) , T.C. Gilliam (2)

1 HMS - Harvard Medical School [Boston]
2 Columbia University [New York]
3 Unict - Università degli studi di Catania = University of Catania
4 St-Luke Roosevelt Hospital

Domaines: Sciences du Vivant [q-bio]

R.E. Tanzi, K. Petrukhin, I. Chernov, J.L. Pellequer, W. Wasco, et al.. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nature Genetics, 1993, 5 (4), pp.344-350. ⟨10.1038/ng1293-344⟩. ⟨hal-03232249⟩