De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment. (2020)
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.59339
Publication URI: https://www.repository.cam.ac.uk/handle/1810/312247
Type: Journal Article/Review