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/10.17863/cam.45123
Publication URI: https://www.repository.cam.ac.uk/handle/1810/298065
Type: Journal Article/Review