Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression. (2017)

First Author: Rocha N

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.7554/eLife.23813

PubMed Identifier: 28414270

Publication URI: http://europepmc.org/abstract/MED/28414270

Type: Journal Article/Review

Volume: 6

Parent Publication: eLife

ISSN: 2050-084X