1.
J Pediatr
; 181: 306-308.e1, 2017 02.
Article
in English
| MEDLINE
| ID: mdl-27931826
ABSTRACT
Mutations in the adenylate cyclase 5 (ADCY5) gene recently have been identified as the cause of a childhood-onset disorder characterized by persistent or paroxysmal choreic, myoclonic, and/or dystonic movements. The 2 novel mutations we identified expand the clinical spectrum of ADCY5 mutations to include alternating hemiplegia of childhood.