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Article

CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation.

Journal of the neurological sciences - 15 Nov 2015

Potic Ana, Nmezi Bruce, Padiath Quasar S

Abstract excerpt

OBJECTIVE: Identification and characterization of a novel pedigree with ATP1A3 mutations presenting with CAPOS syndrome and hemiplegic migraine. METHODS: We have carried out clinical examinations of a three-generation pedigree with CAPOS syndrome and analyzed the ATP1A3 gene to identify causative mutations. The pedigree is of Slavic origin from Southeastern Europe. RESULTS: The clinical phenotype comprised...

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PMID: 26453127
DOI: 10.1016/j.jns.2015.10.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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