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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Shranjeno v:
Bibliografske podrobnosti
izdano v: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
Jezik:Inglês
Izdano: MDPI 2016
Teme:
Review
Online dostop: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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