Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2-Reference-Cited by-同舟云学术

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2

Published:2010-04 Issue:1-2 Volume:291 Page:30-36
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Mantuano Elide,Romano Silvia,Veneziano Liana,Gellera Cinzia,Castellotti Barbara,Caimi Sara,Testa Daniela,Estienne Margherita,Zorzi Giovanna,Bugiani Marianna,Rajabally Yusuf A.,Barcina Maria J Garcìa,Servidei Serena,Panico Aurora,Frontali Marina,Mariotti Caterina

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference32 articles.

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4. Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family;Roubertie;J Neurol,2008

5. Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes;Cuenca-León;Cephalalgia,2008

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