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Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood
Missense mutations in ATP1A3 encoding Na(+),K(+)-ATPase α3 are the primary cause of alternating hemiplegia of childhood (AHC). Most ATP1A3 mutations in AHC lie within a cluster in or near transmembrane α-helix TM6, including I810N that is also found in the Myshkin mouse model of AHC. These mutations...
में बचाया:
| में प्रकाशित: | Neurogenetics |
|---|---|
| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Springer Berlin Heidelberg
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4701769/ https://ncbi.nlm.nih.gov/pubmed/26463346 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-015-0461-1 |
| टैग : |
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