De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Anesthesiology and Pain Medicine,Neurology (clinical),General Medicine
Link
http://link.springer.com/article/10.1186/s10194-017-0770-x/fulltext.html
Reference11 articles.
1. Thomsen LL, Eriksen MK, Roemer SF et al (2002) A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria. Brain 125(Pt 6):1379–1391
2. Di Lorenzo C, Grieco GS, Santorelli FM (2012) Migraine headache: a review of the molecular genetics of a common disorder. J Headache Pain 13(7):571–580 Review
3. Carreño O, Corominas R, Serra SA et al (2013) Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies. Mol Genet Genomic Med 1(4):206–222
4. Riant F, Roze E, Barbance C et al (2012) PRRT2 mutations cause hemiplegic migraine. Neurology 79(21):2122–2124
5. de Vries B, Stam AH, Kirkpatrick M et al (2009) Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. Epilepsia 50(11):2503–2504
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1. Genetics of migraine: complexity, implications, and potential clinical applications;The Lancet Neurology;2024-04
2. Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches;Genes;2024-03-31
3. Clinical features and genetic analysis of two Chinese ATP1A2 gene variants pedigrees of familial hemiplegic migraine;Journal of Neurorestoratology;2023-06
4. Advances in genetics of migraine;The Journal of Headache and Pain;2019-06-21
5. Erratum to: De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report;The Journal of Headache and Pain;2017-07-12
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