Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2

BACKGROUND: The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 (FHM2) are still far from clear. Different ATP1A2 mutations have been described, with a spectrum of phenotypes ranging from mild to severe. No genotype-phenotype correlations have been attempted. CASE...

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Detalles Bibliográficos
Autores principales: Antonaci, Fabio, Ravaglia, Sabrina, Grieco, Gaetano S., Gagliardi, Stella, Cereda, Cristina, Costa, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953819/
https://www.ncbi.nlm.nih.gov/pubmed/33711927
http://dx.doi.org/10.1186/s10194-021-01221-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953819/
https://www.ncbi.nlm.nih.gov/pubmed/33711927
http://dx.doi.org/10.1186/s10194-021-01221-x

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