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Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism.

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Title: Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism.
Authors: Dohrn, Maike F.1,2 (AUTHOR), Bademci, Guney1 (AUTHOR), Rebelo, Adriana P.1 (AUTHOR), Jeanne, Médéric3,4,5 (AUTHOR), Borja, Nicholas A.1 (AUTHOR), Beijer, Danique1 (AUTHOR), Danzi, Matt C.1 (AUTHOR), Bivona, Stephanie A.1 (AUTHOR), Gueguen, Paul3 (AUTHOR), Zafeer, Mohammad F.1 (AUTHOR), Tekin, Mustafa1 (AUTHOR), Züchner, Stephan1 (AUTHOR) szuchner@med.miami.edu, Acosta, Maria T. (AUTHOR), Adams, David R. (AUTHOR), Afzali, Ben (AUTHOR), Allworth, Aimee (AUTHOR), Alvarez, Raquel L. (AUTHOR), Alvey, Justin (AUTHOR), Andrews, Ashley (AUTHOR), Ashley, Euan A. (AUTHOR)
Source: Annals of Clinical & Translational Neurology. Apr2024, Vol. 11 Issue 4, p1075-1079. 5p.
Database: Academic Search Ultimate
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  Data: Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism.
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Clinical+%26+Translational+Neurology%22">Annals of Clinical & Translational Neurology</searchLink>. Apr2024, Vol. 11 Issue 4, p1075-1079. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=176635851
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              Text: Apr2024
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