
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
Keywords: منگنز ; CDG; Congenital Disorders of Glycosylation; UPF0016; Uncharacterized Protein Family 0016; Ca2+; calcium; Mn2+; manganese; GAG; glycosaminoglycans; IEF; isoelectrofocalisation; COG; Conserved Oligomeric Golgi; TMEM165; Gdt1p; Congenital disorders of glycos