Wird geladen...
Mucopolysaccharidosis Type I
Mucopolysaccharidosis type I (MPS I) is caused by the deficiency of α-l-iduronidase, leading to the storage of dermatan and heparan sulfate. There is a broad phenotypical spectrum with the presence or absence of neurological impairment. The classical form is known as Hurler syndrome, the intermediat...
Gespeichert in:
| Veröffentlicht in: | Diagnostics (Basel) |
|---|---|
| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
MDPI
2020
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7151028/ https://ncbi.nlm.nih.gov/pubmed/32188113 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics10030161 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|