A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy
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| Description | scientific article published on 11 August 2019 |
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author: Antonio Vitobello Sébastien Moutton Maurizio Taglialatela |
| Publication date | August 11, 2019 |
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| Missing/wrong data? | Edit Wikidata item |