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/10.1016/j.ajhg.2020.10.012
PubMed Identifier: 33186545
Publication URI: http://europepmc.org/abstract/MED/33186545
Type: Journal Article/Review
Volume: 107
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297