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Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.

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Title: Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
Authors: Pujol‐Giménez, Jonai1,2 (AUTHOR), Mirzaa, Ghayda3,4,5 (AUTHOR), Blue, Elizabeth E.5,6,7 (AUTHOR), Albano, Giuseppe1,2 (AUTHOR), Miller, Danny E.4,5,8 (AUTHOR), Allworth, Aimee6 (AUTHOR), Bennett, James T.3,4,5,9 (AUTHOR), Byers, Peter H.6,8 (AUTHOR), Chanprasert, Sirisak6 (AUTHOR), Chen, Jingheng7 (AUTHOR), Doherty, Daniel4,5 (AUTHOR), Folta, Andrew B.6 (AUTHOR), Gillentine, Madelyn A.10 (AUTHOR), Glass, Ian4,5 (AUTHOR), Hing, Anne4 (AUTHOR), Horike‐Pyne, Martha6 (AUTHOR), Leppig, Kathleen A.11 (AUTHOR), Parhin, Azma6 (AUTHOR), Ranchalis, Jane6 (AUTHOR), Raskind, Wendy H.6 (AUTHOR)
Source: Annals of Clinical & Translational Neurology. Jun2023, Vol. 10 Issue 6, p1046-1053. 8p.
Database: Academic Search Ultimate
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  Data: Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Clinical+%26+Translational+Neurology%22">Annals of Clinical & Translational Neurology</searchLink>. Jun2023, Vol. 10 Issue 6, p1046-1053. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=164352888
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              Text: Jun2023
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              Y: 2023
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