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Functional Consequences of Mutations in the Human α(1A) Calcium Channel Subunit Linked to Familial Hemiplegic Migraine
Mutations in α(1A), the pore-forming subunit of P/Q-type calcium channels, are linked to several human diseases, including familial hemiplegic migraine (FHM). We introduced the four missense mutations linked to FHM into human α(1A-2)subunits and investigated their functional consequences after expre...
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| Foilsithe in: | J Neurosci |
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| Main Authors: | , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Society for Neuroscience
1999
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6782159/ https://ncbi.nlm.nih.gov/pubmed/10024348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.19-05-01610.1999 |
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