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ADCY5 mutations are another cause of benign hereditary chorea. (2015)

First Author: Mencacci NE

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/10.1212/wnl.0000000000001720

PubMed Identifier: 26085604

Publication URI: http://europepmc.org/abstract/MED/26085604

Type: Journal Article/Review

Volume: 85

Parent Publication: Neurology

Issue: 1

ISSN: 0028-3878