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The identification of two pathogenic variants in a family with mild and severe forms of developmental delay | Journal of Human Genetics
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Location of 29 mutations in the KCNQ2 gene and three mutations in the... | Download Scientific Diagram
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FISH mapping of translocation breakpoints reveals truncated KCNQ3 gene... | Download Scientific Diagram
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Relative fold change of the KCNQ1, KCNQ3 and KCNH2 gene expression for... | Download Scientific Diagram
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PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar
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KCNQ gene family members act as both tumor suppressors and oncogenes in gastrointestinal cancers | bioRxiv
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Identification by mass spectrometry and functional characterization of two phosphorylation sites of KCNQ2/KCNQ3 channels | PNAS
![PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f830358b21cb24998a6bfe0e7090a660c4b1bc81/4-Figure1-1.png)
PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar
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Genes and Epilepsy KCNQ3 eBook : Mittal, Mallika, Ahmed, Iqra Eeman, Anwar, Mariam : Amazon.ca: Kindle Store
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KCNQ2 and KCNQ3 polypeptides share a homologous domain near their C... | Download Scientific Diagram
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