Impact, Characterization, and Rescue of Pre-mRNA Splicing Mutations in Lysosomal Storage Disorders

Lysosomal storage disorders (LSDs) represent a group of more than 50 severe metabolic diseases caused by the deficiency of specific lysosomal hydrolases, activators, carriers, or lysosomal integral membrane proteins, leading to the abnormal accumulation of substrates within the lysosomes. Numerous m...

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Detalles Bibliográficos
Autores principales: Dardis, Andrea, Buratti, Emanuele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852569/
https://www.ncbi.nlm.nih.gov/pubmed/29415500
http://dx.doi.org/10.3390/genes9020073

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852569/
https://www.ncbi.nlm.nih.gov/pubmed/29415500
http://dx.doi.org/10.3390/genes9020073

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