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/10.17863/cam.83247

Publication URI: https://www.repository.cam.ac.uk/handle/1810/335811

Type: Journal Article/Review