Mouse models for congenital disorders of glycosylation

Journal of Inherited Metabolic Disease

Volumn 34, Issue 4, 2011, Pages 879-889

  Thiel, Christian ^a   Körner, Christian ^a  

^a Center for Metabolic Diseases Heidelberg   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE DIPHOSPHATE FUCOSE; MANNOSE 6 PHOSPHATE; MANNOSE PHOSPHATE ISOMERASE; N ACETYLGLUCOSAMINYLTRANSFERASE; N ACETYLLACTOSAMINE SYNTHASE; PHOSPHOMANNOMUTASE; PHOSPHOMANNOMUTASE 2; UNCLASSIFIED DRUG; URIDINE DIPHOSPHATE N ACETYLGLUCOSAMINE;

AUTOSOMAL RECESSIVE DISORDER; CONGENITAL DISORDER OF GLYCOSYLATION; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1A; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1B; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1J; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1Q; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2A; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2C; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2D; DISEASE MODEL; EMBRYO DEVELOPMENT; ENZYME ACTIVITY; ENZYME PHOSPHORYLATION; GENE DELETION; GENE DISRUPTION; GENE MUTATION; GESTATIONAL AGE; GLYCOPROTEIN SYNTHESIS; GOLGI COMPLEX; HUMAN; MOLECULAR PATHOLOGY; NEUROLOGIC DISEASE; NONHUMAN; POSTNATAL DEVELOPMENT; PROTEIN GLYCOSYLATION; PROTEIN PROCESSING; REVIEW; SYSTEMIC DISEASE;

3-OXO-5-ALPHA-STEROID 4-DEHYDROGENASE; ANIMALS; CONGENITAL DISORDERS OF GLYCOSYLATION; DISEASE MODELS, ANIMAL; HUMANS; MICE; MICE, TRANSGENIC; MODELS, BIOLOGICAL; PHOSPHOTRANSFERASES (PHOSPHOMUTASES);

EID: 79961171857     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-011-9295-7     Document Type: Review

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