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2020 | 1 |
2021 | 1 |
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Movement disorders rounds: Atypical cases in two Chinese families with novel variants in ATP1A3.
Parkinsonism Relat Disord. 2020 Sep;78:189-191. doi: 10.1016/j.parkreldis.2020.05.030. Epub 2020 Jun 29.
Parkinsonism Relat Disord. 2020.
PMID: 32684337
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Vetro A, Nielsen HN, Holm R, Hevner RF, Parrini E, Powis Z, Møller RS, Bellan C, Simonati A, Lesca G, Helbig KL, Palmer EE, Mei D, Ballardini E, Van Haeringen A, Syrbe S, Leuzzi V, Cioni G, Curry CJ, Costain G, Santucci M, Chong K, Mancini GMS, Clayton-Smith J, Bigoni S, Scheffer IE, Dobyns WB, Vilsen B, Guerrini R; ATP1A2/A3-collaborators.
Vetro A, et al.
Brain. 2021 Jun 22;144(5):1435-1450. doi: 10.1093/brain/awab052.
Brain. 2021.
PMID: 33880529
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