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TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (2022)

First Author: Tábara L

Attributed to: Precision Medicine Exeter Innovation Platform (PMEI Platform) 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

Parent Publication: Brain

Issue: 9

ISSN: 0006-8950