| 1 | CDG2K, TMEM165 |
| TMEM165 deficiencies in Congenital Disorders of Glycosylation type II (CDG-II): Clues and evidences for roles of the protein in Golgi functions and ion homeostasis. | |
| Dulary E, Potelle S, Legrand D, Foulquier F. | |
| Tissue Cell. Apr;49(2 Pt A):150-156. doi: 10.1016/j.tice.2016.06.006. Epub 2016 Jun 16 2017 | |
| 2 | CDG2K, TMEM165 |
| Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II | |
| Rosnoblet C, Legrand D, Demaegd D, Hacine-Gherbi H, de Bettignies G, Bammens R, Borrego C, Duvet S, Morsomme P, Matthijs G, Foulquier F. | |
| Hum Mol Genet. Jul 15;22(14):2914-28. doi: 10.1093/hmg/ddt146. Epub 2013 Apr 10. 2013 | |
| 3 | CDG2K, TMEM165 |
| TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation. | |
| Foulquier F, Amyere M, Jaeken J, Zeevaert R, Schollen E, Race V, Bammens R, Morelle W, Rosnoblet C, Legrand D, Demaegd D, Buist N, Cheillan D, Guffon N, Morsomme P, Annaert W, Freeze HH, Van Schaftingen E, Vikkula M, Matthijs G. | |
| Am J Hum Genet 91(1):15-26. Epub 2012 Jun 7. 2012 | |