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A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. (2015)

First Author: Mencacci NE

Attributed to: ERANET 1 NEURON 3: Identification of copy number variants in familial and pathologically proven PD funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2015.04.008

PubMed Identifier: 25983243

Publication URI: http://europepmc.org/abstract/MED/25983243

Type: Journal Article/Review

Volume: 96

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297