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Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features. (2021)

First Author: Benincá C

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