Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
About this item
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Author / Creator
Publisher
United States: Columbia University Libraries/Information Services
Journal title
Language
English
Formats
Publication information
Publisher
United States: Columbia University Libraries/Information Services
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Scope and Contents
Contents
Paroxysmal movement disorders are rare and heterogeneous genetic conditions characterized by the recurrence of transient involuntary movements.
The phenomenology of a paroxysmal kinesigenic dyskinesia in a young professional athlete.
Providing basic clinical and genetic elements for the early recognition and diagnosis of a rare movement disor...
Alternative Titles
Full title
Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
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TN_cdi_doaj_primary_oai_doaj_org_article_b7f0af67c7df4a85b291e7c244e40a34
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b7f0af67c7df4a85b291e7c244e40a34
Other Identifiers
ISSN
2160-8288
E-ISSN
2160-8288
DOI
10.7916/D8S488X0
