Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease

Por Merle, Uta, Weiss, Karl Heinz, Eisenbach, Christoph, Tuma, Sabine, Ferenci, Peter, Stremmel, Wolfgang
Publicado em 2010

Copper-Induced Translocation of the Wilson Disease Protein ATP7B Independent of Murr1/COMMD1 and Rab7

Por Weiss, Karl Heinz, Lozoya, Javier Carbajo, Tuma, Sabine, Gotthardt, Daniel, Reichert, Jürgen, Ehehalt, Robert, Stremmel, Wolfgang, Füllekrug, Joachim
Publicado em 2008