Abstract
Familial hemiplegic migraine type 1 (FHM1) is caused by missense mutations in the CACNA1A gene that encodes the α1A pore-forming subunit of Ca
| Original language | English |
|---|---|
| Pages (from-to) | 2531-2535 |
| Journal | Journal of Proteomics |
| Volume | 10 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - 2010 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 10 Reduced Inequalities
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