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Phosphomannomutase deficiency is the main cause of carbohydr…
Phosphomannomutase deficiency is the main cause of carbohydrate deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins
Phosphomannomutase deficiency is the main cause of carbohydrate deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins
Article, Chapter
Authors: Jaeken
Publication: Journal of Inherited Metabolic Disease
Published: Springer Netherlands
ISSN: 0141-8955
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View Full Text Source:Journal of Inherited Metabolic Disease,Journal of Inherited Metabolic Disease,Springer Complete Journals Opens in new Window
Journal:  Journal of Inherited Metabolic Disease Source:Springer Complete Journals Opens in new Window
Collection:  Springer Complete Journals Opens in new Window
Coverage:
  • 1978-03-01~2018-11-01; volume:1;issue:1~volume:41;issue:6
View Full Text Source:Journal of Inherited Metabolic Disease,Journal of Inherited Metabolic Disease,Wiley Online Library: Complete Journals Opens in new Window
Journal:  Journal of Inherited Metabolic Disease Source:Wiley Online Library: Complete Journals Opens in new Window
Collection:  Wiley Online Library: Complete Journals Opens in new Window
Coverage:
  • 1997-02-01~present; volume:20~present
View Full Text Source:Journal of Inherited Metabolic Disease,Journal of Inherited Metabolic Disease,Wiley Online Library Database Model 2021 Opens in new Window
Journal:  Journal of Inherited Metabolic Disease Source:Wiley Online Library Database Model 2021 Opens in new Window
Collection:  Wiley Online Library Database Model 2021 Opens in new Window
Coverage:
  • 1997~present; volume:20~present;issue:1~present
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