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Published in 2020 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-020-01594-3
Abstract: Background GNAO1 encephalopathy is a rare neurodevelopmental disorder characterized by distinct movement presentations and early onset epileptic encephalopathy. Here, we report the in-depth phenotyping of genetically confirmed patients with GNAO1 encephalopathy, focusing on movement presentations.…
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Keywords:
movement;
gnao1 encephalopathy;
case;
spectrum movement ... See more keywords