Crosstalk between 2 organelles: Lysosomal storage of heparan sulfate causes mitochondrial defects and neuronal death in mucopolysaccharidosis III type C

More than 30% of all lysosomal diseases are mucopolysaccharidoses, disorders affecting the enzymes needed for the stepwise degradation of glycosaminoglycans (mucopolysaccharides). Mucopolysaccharidosis type IIIC (MPS IIIC) is a severe neurologic disease caused by genetic deficiency of heparan sulfat...

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Detalles Bibliográficos
Autor principal: Pshezhetsky, Alexey V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588229/
https://www.ncbi.nlm.nih.gov/pubmed/26459666
http://dx.doi.org/10.1080/21675511.2015.1049793

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588229/
https://www.ncbi.nlm.nih.gov/pubmed/26459666
http://dx.doi.org/10.1080/21675511.2015.1049793

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