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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...
Gorde:
| Argitaratua izan da: | J Headache Pain |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Springer Milan
2021
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7953819/ https://ncbi.nlm.nih.gov/pubmed/33711927 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s10194-021-01221-x |
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