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Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation. (2014)

First Author: Dusi S

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.11.008

PubMed Identifier: 24360804

Publication URI: http://europepmc.org/abstract/MED/24360804

Type: Journal Article/Review

Volume: 94

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297