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Causative Role of the SLC6A1 p.Asp451Gly Variant in a Patient with Combined Dystonia and Neurodevelopmental Disorder.

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Bibliographic Details
Title: Causative Role of the SLC6A1 p.Asp451Gly Variant in a Patient with Combined Dystonia and Neurodevelopmental Disorder.
Authors: Romito, Luigi M.1,2 (AUTHOR) luigi.romito@istituto-besta.it, Colucci, Fabiana1,3 (AUTHOR), Leta, Valentina1,4 (AUTHOR), Panteghini, Celeste5 (AUTHOR), Telese, Roberta1,6 (AUTHOR), Tolva, Gianluca7 (AUTHOR), Villa, Roberta7 (AUTHOR), Elia, Antonio E.1 (AUTHOR), Eleopra, Roberto1 (AUTHOR), Peron, Angela8 (AUTHOR), Garavaglia, Barbara5 (AUTHOR), Iascone, Maria9 (AUTHOR)
Source: Movement Disorders Clinical Practice. Feb2025, Vol. 12 Issue 2, p239-241. 3p.
Database: Academic Search Ultimate
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ISSN:23301619
DOI:10.1002/mdc3.14246