A Distinct Phenotype in a Novel ATP1A3 Mutation: Connecting the Two Ends of a Spectrum

Mov Disord Clin Pract. 2015 Nov 28;3(4):398-401. doi: 10.1002/mdc3.12263. eCollection 2016 Jul-Aug.

Authors

Pedro Pereira¹, Andreia Guerreiro², Maria Fonseca³, Cristina Halpern³, Jorge Pinto-Basto⁴, José P Monteiro³

Affiliations

¹ Neurology Department Hospital Garcia de Orta Almada Portugal.
² Pediatrics Department Hospital Garcia de Orta Almada Portugal.
³ Center for Child Development Torrado da Silva Hospital Garcia de Orta Almada Portugal.
⁴ Clinical Genetics Department Centro de Genética Clínica Porto Portugal.

No abstract available

Keywords: alternating hemiplegia of childhood; intermediate phenotype; rapid‐onset dystonia‐parkinsonism.

Publication types

Case Reports