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Alterations in the α2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2
A number of missense mutations in the Na,K-ATPase α2 catalytic subunit have been identified in familial hemiplegic migraine with aura. Two alleles (L764P and W887R) showed loss-of-function, whereas a third (T345A) is fully functional but with altered Na,K-ATPase kinetics. This study describes two ad...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
National Academy of Sciences
2005
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1178013/ https://ncbi.nlm.nih.gov/pubmed/16037212 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0504323102 |
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