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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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Bibliografiske detaljer
Udgivet i:Diseases
Main Authors: 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
Format: Artigo
Sprog:Inglês
Udgivet: MDPI 2016
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5456326/
https://ncbi.nlm.nih.gov/pubmed/28933411
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diseases4040031
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