Mitochondrial Dysfunction in Lysosomal Storage Disorders

Lysosomal storage diseases (LSDs) describe a heterogeneous group of rare inherited metabolic disorders that result from the absence or loss of function of lysosomal hydrolases or transporters, resulting in the progressive accumulation of undigested material in lysosomes. The accumulation of substanc...

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Detalles Bibliográficos
Autores principales: de la Mata, Mario, Cotán, David, Villanueva-Paz, Marina, de Lavera, Isabel, Álvarez-Córdoba, Mónica, Luzón-Hidalgo, Raquel, Suárez-Rivero, Juan M., Tiscornia, Gustavo, Oropesa-Ávila, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456326/
https://www.ncbi.nlm.nih.gov/pubmed/28933411
http://dx.doi.org/10.3390/diseases4040031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456326/
https://www.ncbi.nlm.nih.gov/pubmed/28933411
http://dx.doi.org/10.3390/diseases4040031

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