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Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. (2013)

First Author: Silveira-Moriyama L

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/10.1111/dmcn.12056

PubMed Identifier: 23363396

Publication URI: http://europepmc.org/abstract/MED/23363396

Type: Journal Article/Review

Volume: 55

Parent Publication: Developmental medicine and child neurology

Issue: 4

ISSN: 0012-1622