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Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. (2013)

First Author: Bonnen PE

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.07.017

PubMed Identifier: 23993193

Publication URI: http://europepmc.org/abstract/MED/23993193

Type: Journal Article/Review

Volume: 93

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297