Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. (2014)

First Author: Logan CV
Attributed to:  Ciliopathy disease gene identification by whole exome medical resequencing funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.2851

PubMed Identifier: 24336167

Publication URI: http://europepmc.org/abstract/MED/24336167

Type: Journal Article/Review

Volume: 46

Parent Publication: Nature genetics

Issue: 2

ISSN: 1061-4036