Digestive and Liver Disease
 2017
DOI: 10.1016/j.dld.2017.09.021
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Three patients with glycosylation deficiencies, chronically elevated transaminases, and low serum ceruloplasmin and copper, caused by mutations in the gene encoding the transmembrane protein TMEM199

Marco Poeta
1
,
K Zielińska
2
,
Marco Maccarana
3
et al.
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