Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases

INTRODUCTION: Lysosomal storage diseases (LSDs) are rare inherited metabolic diseases characterized by an abnormal accumulation of various toxic materials in the cells as a result of enzyme deficiencies leading to tissue and organ damage. Among clinical manifestations, cardiac diseases are particula...

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Detalles Bibliográficos
Autores principales: Belfiore, Maria Paola, Iacobellis, Francesca, Acampora, Emma, Caiazza, Martina, Rubino, Marta, Monda, Emanuele, Magaldi, Maria Rosaria, Tarallo, Antonietta, Sasso, Marcella, De Pasquale, Valeria, Grassi, Roberto, Cappabianca, Salvatore, Calabrò, Paolo, Fecarotta, Simona, Esposito, Salvatore, Esposito, Giovanni, Pisani, Antonio, Pavone, Luigi Michele, Parenti, Giancarlo, Limongelli, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236983/
https://www.ncbi.nlm.nih.gov/pubmed/32428018
http://dx.doi.org/10.1371/journal.pone.0233050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236983/
https://www.ncbi.nlm.nih.gov/pubmed/32428018
http://dx.doi.org/10.1371/journal.pone.0233050

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