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Open Access 01-12-2015 | Poster presentation

P016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report

Authors: Roberto Frusciante, Alessandro Capuano, Lorena Travaglini, Ginevra Zanni, Federico Vigevano, Enrico Bertini, Massimiliano Valeriani

Published in: The Journal of Headache and Pain | Special Issue 1/2015

Excerpt

The CACNA1A gene encodes the pore forming alpha-1A subunit of neuronal voltage-dependent P/Q-type Ca (2+) channels. Mutations in this gene result in clinical heterogeneity, including hemiplegic migraine, episodic ataxia, or progressive chronic conditions. …

Title: P016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report
Authors: Roberto Frusciante
Alessandro Capuano
Lorena Travaglini
Ginevra Zanni
Federico Vigevano
Enrico Bertini
Massimiliano Valeriani
Publication date: 01-12-2015
Publisher: Springer Milan
Published in: The Journal of Headache and Pain / Issue Special Issue 1/2015
Print ISSN: 1129-2369
Electronic ISSN: 1129-2377
DOI: https://doi.org/10.1186/1129-2377-16-S1-A146

At a glance: The STEP trials

Springer Medicine

P016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report

Excerpt

At a glance: The STEP trials

Springer Medicine

Excerpt

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