Lysosomal storage diseases as a complex pathophysiological and clinical problem - part one

Lysosomal storage diseases (LSDs) are a group of rare genetic diseases that are characterized by the accumulation of undecomposed molecules in lysosomes due to deficits in specific enzymes. One of the most common subtypes of LSDs is mucopolysaccharidoses (MPS), in which there is an accumulation of...

Full description

Saved in:
Bibliographic Details
Main Author: Karolina Mikołajczak
Format: Article
Language:English
Published: Nicolaus Copernicus University in Toruń 2025-05-01
Series:Quality in Sport
Subjects:
Online Access:https://apcz.umk.pl/QS/article/view/59859
Tags: Add Tag
No Tags, Be the first to tag this record!