| 1 | ATP1A3, CAPOS
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| The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
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| Sweney MT, Newcomb TM, Swoboda KJ.
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| Pediatr Neurol 52(1):56-64. doi: 10.1016/j.pediatrneurol.2014.09.015. Epub 2014 Oct 13. Review.
2015
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| 2 | ATP1A3, CAPOS
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| CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation.
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| Potic A, Nmezi B, Padiath QS.
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| J Neurol Sci 358(1-2):453-6. doi: 10.1016/j.jns.2015.10.002. Epub 2015 Oct 3.
2015
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| 3 | ATP1A3, CAPOS
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| A novel recurrent mutation in ATP1A3 causes CAPOS syndrome.
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| Demos MK, van Karnebeek CD, Ross CJ, Adam S, Shen Y, Zhan SH, Shyr C, Horvath G, Suri M, Fryer A, Jones SJ, Friedman JM; FORGE Canada Consortium.
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| Orphanet J Rare Dis 9:15. doi: 10.1186/1750-1172-9-15.
2014
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| 4 | CAPOS
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| Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome.
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| Rosewich H, Weise D, Ohlenbusch A, Gärtner J, Brockmann K.
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| Neurology 83(9):861-3. doi: 10.1212/WNL.0000000000000735. Epub 2014 Jul 23. No abstract available.
2014
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