Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies-Reference-Cited by-同舟云学术

Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies

Published:2013-07-02 Issue:4 Volume:1 Page:206-222
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Carreño Oriel¹²³,Corominas Roser¹³⁴,Serra Selma Angèlica⁵,Sintas Cèlia¹²³,Fernández‐Castillo Noèlia¹²³,Vila‐Pueyo Marta⁴,Toma Claudio¹²³,Gené Gemma G.⁵,Pons Roser⁶,Llaneza Miguel⁷,Sobrido María‐Jesús³⁸,Grinberg Daniel¹²³,Valverde Miguel Ángel⁵,Fernández‐Fernández José Manuel⁵,Macaya Alfons⁴,Cormand Bru¹²³

Affiliation:

1. Departament de Genètica Facultat de Biologia Universitat de Barcelona Barcelona Spain

2. Institut de Biomedicina de la Universitat de Barcelona (IBUB) Barcelona Spain

3. Center for Biomedical Network Research on Rare Diseases (CIBERER) Institute of Health Carlos III Spain

4. Pediatric Neurology Research Group Vall d'Hebron Research Institute Universitat Autònoma de Barcelona Barcelona Spain

5. Laboratory of Molecular Physiology and Channelopathies Department of Experimental and Health Sciences Universitat Pompeu Fabra Barcelona Spain

6. First Department of Pediatrics Agia Sofia Hospital University of Athens Athens Greece

7. Sección de Neurología Complejo Hospitalario Arquitecto Marcide‐Novoa Santos Ferrol Spain

8. Fundación Pública Galega de Medicina Xenómica Santiago de Compostela Spain

Funder

Spanish Ministry of Science and Innovation

Spanish Ministry of Economy and Competitiveness

Fondos Europeos de Desarrollo Regional (FEDER) and Plan E

Fondo de Investigación Sanitaria

Generalitat de Catalunya

CIBER-ER

European Union

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.24

Reference83 articles.

1. Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel

2. Phenotypes of Spinocerebellar Ataxia Type 6 and Familial Hemiplegic Migraine Caused by a Unique CACNA1A Missense Mutation in Patients From a Large Family

3. A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

4. A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

5. Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

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5. Concomitant Calcium Channelopathies Involving CACNA1A and CACNA1F: A Case Report and Review of the Literature;Genes;2023-02-03