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.