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AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome (2017)

First Author: Di Meo I

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/10.1038/gt.2017.53

Publication URI: http://dx.doi.org/10.1038/gt.2017.53

Type: Journal Article/Review

Parent Publication: Gene Therapy

Issue: 10