Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features. (2021)
Attributed to:
Investigation of the function of the ER/mitochondria contact sites in cell physiology and disease
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2020-106861
PubMed Identifier: 32439808
Publication URI: http://europepmc.org/abstract/MED/32439808
Type: Journal Article/Review
Volume: 58
Parent Publication: Journal of medical genetics
Issue: 3
ISSN: 0022-2593