Results
eNauka >
Results >
Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia
| Title: | Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia | Authors: | Hedera, Peter; Xiao, Jianfeng; Puschmann, Andreas; Momcilovic, Dragana R; Wu, Steve W; LeDoux, Mark S | Issue Date: | 2012 | Publication: | BMC NEUROLOGY | ISSN: | 1471-2377 BMC Neurology Search Idenfier |
Type: | Article | Collation: | vol. 12 br. 1 | DOI: | 10.1186/1471-2377-12-93 | WoS-ID: | 000309394700001 | Scopus-ID: | 2-s2.0-84866279746 | URI: | https://enauka.gov.rs/handle/123456789/819824 | Project: | Neuroscience Institute Dystonia Medical Research Foundation NIH [R01NS048458, R01NS069936] NIH Dystonia Coalition Pilot Projects Program [U54NS065701] NIH/NINDS [K02NS057666] Swedish National Health Services Swedish Parkinson Foundation (Parkinsonfo |
Metadata source: | (Preuzeto iz Nasi u WoS) | M-category: | 21M21 |
Items in eNauka are protected by copyright, with all rights reserved, unless otherwise indicated.