Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features. (2020)
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/10.17863/cam.56197
Publication URI: https://www.repository.cam.ac.uk/handle/1810/309103
Type: Journal Article/Review