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1734516
1734516
https://w3id.org/oc/corpus/br/1734516
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
P3181
adaceaeeffa0d620c023d5e4b22908cdd770d67e
P3181
Q24600816-EFF122E2-80E5-4AFC-9F88-547F0D380570
P3181
1734516
https://w3id.org/oc/corpus/br/1734516