Mitochondrial Dysfunction in Lysosomal Storage Disorders

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...

Full description

Bibliographic Details
Main Authors: Mario de la Mata, David Cotán, Marina Villanueva-Paz, Isabel de Lavera, Mónica Álvarez-Córdoba, Raquel Luzón-Hidalgo, Juan M. Suárez-Rivero, Gustavo Tiscornia, Manuel Oropesa-Ávila
Format: Article
Language:English
Published: MDPI AG 2016-10-01
Series:Diseases
Subjects:
lysosomal storage disorders
mitochondrial dysfunction
Gaucher disease
Online Access:http://www.mdpi.com/2079-9721/4/4/31

Internet

http://www.mdpi.com/2079-9721/4/4/31

Similar Items