Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy
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| Description | scientific article published in 2022 |
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author: Antonio Vitobello Anne-Sophie Denommé-Pichon Rami Abou Jamra Johannes R Lemke Heinrich Sticht Konrad Platzer |
| Publication date | December 23, 2022 |
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