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3. Mouse models characterize GNAO1 encephalopathy as a neurodevelopmental disorder leading to motor anomalies: from a severe G203R to a milder C215Y mutation. Silachev D; Koval A; Savitsky M; Padmasola G; Quairiaux C; Thorel F; Katanaev VL Acta Neuropathol Commun; 2022 Jan; 10(1):9. PubMed ID: 35090564 [TBL] [Abstract][Full Text] [Related]
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