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Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy
scientific article published in 2022
Author/s
author: Heinrich Sticht, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Johannes R Lemke, Rami Abou Jamra, Platzer K
Work details
Publication date
December 23, 2022
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Language
English
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