Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: A Critical Review with Future Perspectives

Lysosomal storage disorders (LSDs) are predominantly very rare recessive autosomal neurodegenerative diseases.Sphingolipidoses, a sub-group of LSDs, result from defects in lysosomal enzymes involved in sphingolipid catabolism, and feature disrupted storage systems which trigger complex pathogenic ca...

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Detalles Bibliográficos
Autores principales: Percival, Benita Claire, Gibson, Miles, Wilson, Philippe B., Platt, Frances M., Grootveld, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178094/
https://www.ncbi.nlm.nih.gov/pubmed/32260582
http://dx.doi.org/10.3390/ijms21072533

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178094/
https://www.ncbi.nlm.nih.gov/pubmed/32260582
http://dx.doi.org/10.3390/ijms21072533

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