Recent trends in mucopolysaccharidosis research

Mucopolysaccharidosis (MPS) is a group of inherited conditions involving metabolic dysfunction. Lysosomal enzyme deficiency leads to the accumulation of glycosaminoglycan (GAG) resulting in systemic symptoms, and is categorized into seven types caused by deficiency in one of eleven different enzymes...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of human genetics 2019-02, Vol.64 (2), p.127-137
1. Verfasser:	Kobayashi, Hiroshi
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Antigens Astrocytes Autophagy Blood-brain barrier Brain stem Cell cycle Combined Modality Therapy Diagnosis, Differential Disease Enzyme Replacement Therapy Enzymes Gene expression Gene therapy Genetic Association Studies Genetic disorders Genetic Therapy Genome editing Genomes Genotype & phenotype Glycosaminoglycans Hematopoietic Stem Cell Transplantation Hematopoietic stem cells Heparan sulfate Humans Inflammation Metabolic disorders Metabolism Microglia Mucopolysaccharidoses - diagnosis Mucopolysaccharidoses - etiology Mucopolysaccharidoses - metabolism Mucopolysaccharidoses - therapy Mucopolysaccharidosis Neurodegenerative diseases Phagocytosis Phenotype Prevalence Stem cell transplantation Tau protein Trends
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!