Spastin MIT Domain Disease-Associated Mutations Disrupt Lysosomal Function. (2019)
Attributed to:
Investigating lysosomal dysfunction as a unifying pathological mechanism in hereditary spastic paraplegia
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.3389/fnins.2019.01179
PubMed Identifier: 31787869
Publication URI: http://europepmc.org/abstract/MED/31787869
Type: Journal Article/Review
Volume: 13
Parent Publication: Frontiers in neuroscience
ISSN: 1662-453X