Condition: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If


rs104894589 in LOC100996842;MPDU1 gene and CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If PMID 11733564 2001 MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.

PMID 11733556 2001 A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If).

rs104894587 in MPDU1 gene and CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If PMID 11733556 2001 A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If).

PMID 11733564 2001 MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.

rs104894586 in MPDU1;LOC100996842 gene and CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If PMID 11733556 2001 A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If).

PMID 11733564 2001 MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.