Potelle, Sven <br/><br/>
Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis.  [electronic resource] 

 -  Human molecular genetics  Apr 2016 
 - 1489-500 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddw026  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antiporters<br/>Cation Transport Proteins<br/>Congenital Disorders of Glycosylation--genetics<br/>Fungal Proteins--genetics<br/>Glycosylation--drug effects<br/>Golgi Apparatus--drug effects<br/>HEK293 Cells<br/>HeLa Cells<br/>Homeostasis<br/>Humans<br/>Manganese--metabolism<br/>Membrane Proteins--deficiency<br/>Mutation<br/>Vesicular Transport Proteins--metabolism