TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia. (2022)
Attributed to:
Precision Medicine Exeter Innovation Platform (PMEI Platform): Proof of Concept Funds
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awac123
PubMed Identifier: 35718349
Publication URI: http://europepmc.org/abstract/MED/35718349
Type: Journal Article/Review
Volume: 145
Parent Publication: Brain : a journal of neurology
Issue: 9
ISSN: 0006-8950