Related references
Note: Only part of the references are listed.Dolichol-phosphate mannose synthase: Structure, function and regulation
Yusuke Maeda et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2008)
Clinical and molecular characterization of the first adult congenital disorder of glycosylation (CDG) type Ic patient
LW Sun et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
CDG-IL:: An infant with a novel mutation in the ALG9 gene and additional phenotypic features
M Weinstein et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
B Schenk et al.
JOURNAL OF CLINICAL INVESTIGATION (2001)
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)
C Kranz et al.
JOURNAL OF CLINICAL INVESTIGATION (2001)
Requirement of the Lec35 gene for all known classes of monosaccharide-P-dolichol-dependent glycosyltransferase reactions in mammals
M Anand et al.
MOLECULAR BIOLOGY OF THE CELL (2001)
Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylation
V Westphal et al.
AMERICAN JOURNAL OF PATHOLOGY (2000)
Share Paper
