@article{ATM22837,
author = {Ralf Weiskirchen and Wolfgang Stremmel},
title = {Editorial for focused issue “Wilson Disease: From Genetics to Management of Disease”},
journal = {Annals of Translational Medicine},
volume = {7},
number = {Suppl 2},
year = {2018},
keywords = {},
abstract = {Wilson disease was previously called hepatolenticular degeneration. It is a rare inherited disorder preventing the body from removing copper via bile. Accordingly, copper builds up in liver and spills over to other organs, i.e., the basal ganglia of the brain.},
issn = {2305-5847}, url = {https://atm.amegroups.org/article/view/22837}
}