Amanote Research
Register
Sign In
Congenital Disorder of Glycosylation
doi 10.32388/kehi7p
Full Text
Open PDF
Abstract
Available in
full text
Date
February 10, 2020
Authors
Unknown
Publisher
Qeios
Related search
Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation
American Journal of Human Genetics
Genetics
Clinical Utility Gene Card For: GALNT3 Defective Congenital Disorder of Glycosylation
European Journal of Human Genetics
Genetics
Anesthetic Management of a Boy With Congenital Disorder of Glycosylation (CDG) I-X
International Journal of Clinical Medicine
MPDU1 Mutations Underlie a Novel Human Congenital Disorder of Glycosylation, Designated Type If
Journal of Clinical Investigation
Medicine
Congenital Disorders of Glycosylation. Part II. Defects of Protein O-Glycosylation.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
Deficiency of Dolichyl-P-Man:Man7GlcNAc2-Pp-Dolichyl Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ig
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Congenital Disorder of Glycosylation Type Ia (CDG-Ia): Phenotypic Spectrum of the R141h/F119l Genotype
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Congenital Disorders of Glycosylation. Part I. Defects of Protein N-Glycosylation.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
PO-0827 Conotruncal Heart Defect in a Patient With Congenital Disorder of Glycosylation Type I
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology