Evaluation of Cell Models to Study Monocyte Functions in PMM2 Congenital Disorders of Glycosylation

Congenital disorders of glycosylation (CDG) are inherited metabolic diseases characterized by mutations in enzymes involved in different steps of protein glycosylation, leading to aberrant synthesis, attachment or processing of glycans. Recently, immunological dysfunctions in several CDG types have...

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Detalles Bibliográficos
Autores principales: de Haas, Paola, de Jonge, Marien I., Koenen, Hans J. P. M., Joosten, Ben, Janssen, Mirian C. H., de Boer, Lonneke, Hendriks, Wiljan J. A. J., Lefeber, Dirk J., Cambi, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121068/
https://www.ncbi.nlm.nih.gov/pubmed/35603178
http://dx.doi.org/10.3389/fimmu.2022.869031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121068/
https://www.ncbi.nlm.nih.gov/pubmed/35603178
http://dx.doi.org/10.3389/fimmu.2022.869031

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