Lack of significant ganglioside changes in Slc17a5 heterozygous mice: Relevance to FSASD and Parkinson's disease

Lack of significant ganglioside changes in Slc17a5 heterozygous mice: Relevance to FSASD and Parkinson's disease

Large population-based studies of Parkinson's disease (PD) have identified susceptibility genes, including SLC17A5. Biallelic mutations in SLC17A5, encoding the lysosomal sialic acid transporter sialin, cause the rare neurodegenerative disease, free sialic acid storage disorder (FSASD). To expl...

Full description

Saved in:
Bibliographic Details
Main Authors: Marya S. Sabir, Mahin S. Hossain, Laura Pollard, Marjan Huizing, William A. Gahl, Frances M. Platt, May Christine V. Malicdan
Format: Article
Language:English
Published: Elsevier 2025-06-01
Series:Biochemistry and Biophysics Reports
Subjects:
Parkinson's disease
Salla disease
SLC17A5
Sialin
Glycosphingolipids
Mouse model
Online Access:http://www.sciencedirect.com/science/article/pii/S2405580825000664
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items

Similar Items