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Paper Details

TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Brain
16
2022
Author NameAffiliation
Henry HouldenUCL Queen Square Institute of Neurology, University College London
Emma L BapleRILD Wellcome Wolfson Medical Research Centre, RD&E (Wonford) NHS Foundation Trust, University of Exeter Medical School
Emma L BaplePeninsula Clinical Genetics Service, Royal Devon and Exeter Hospital (Heavitree)
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