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A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy
scientific article published on 11 August 2019
Author/s
author: Sébastien Moutton, Antonio Vitobello, Maurizio Taglialatela
Work details
Publication date
August 11, 2019
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Language
English
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