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Author Podcast: Alice Gardiner

'Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations'


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Subtitle: 'Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations'
Summary: To define better the phenotype and genotype of familial and sporadic cases of paroxysmal kinesigenic dyskinesia (PKD) caused by mutations in the PRRT2 gene presenting in the paediatric age group.
Author: wileyblackwellhealth; Category: Health; Explicit: No

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/ 0:01:4401280.0116.55 MB
Alice Gardiner discusses the article 'Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations'

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