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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2014 | 1 |
2015 | 2 |
2016 | 1 |
2024 | 0 |
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Distinct neurological disorders with ATP1A3 mutations.
Lancet Neurol. 2014 May;13(5):503-14. doi: 10.1016/S1474-4422(14)70011-0.
Lancet Neurol. 2014.
PMID: 24739246
Free PMC article.
Review.
Functional Studies of Na(+),K(+)-ATPase Using Transfected Cell Cultures.
Arystarkhova E, Sweadner KJ.
Arystarkhova E, et al.
Methods Mol Biol. 2016;1377:321-32. doi: 10.1007/978-1-4939-3179-8_28.
Methods Mol Biol. 2016.
PMID: 26695043
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Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly.
Paciorkowski AR, McDaniel SS, Jansen LA, Tully H, Tuttle E, Ghoneim DH, Tupal S, Gunter SA, Vasta V, Zhang Q, Tran T, Liu YB, Ozelius LJ, Brashear A, Sweadner KJ, Dobyns WB, Hahn S.
Paciorkowski AR, et al.
Epilepsia. 2015 Mar;56(3):422-30. doi: 10.1111/epi.12914. Epub 2015 Feb 5.
Epilepsia. 2015.
PMID: 25656163
Free PMC article.
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A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1.
Liu YB, Tewari A, Salameh J, Arystarkhova E, Hampton TG, Brashear A, Ozelius LJ, Khodakhah K, Sweadner KJ.
Liu YB, et al.
Elife. 2015 Dec 24;4:e11102. doi: 10.7554/eLife.11102.
Elife. 2015.
PMID: 26705335
Free PMC article.
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