Expanding the genotype and phenotype spectrum of SYT1-associated neurodevelopmental disorder

PURPOSE: Synaptotagmin-1 (SYT1) is a critical mediator of neurotransmitter release in the central nervous system. Previously reported missense SYT1 variants in the C2B domain are associated with severe intellectual disability, movement disorders, behavioral disturbances, and electroencephalogram abn...

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Detalles Bibliográficos
Autores principales: Melland, Holly, Bumbak, Fabian, Kolesnik-Taylor, Anna, Ng-Cordell, Elise, John, Abinayah, Constantinou, Panayiotis, Joss, Shelagh, Larsen, Martin, Fagerberg, Christina, Laulund, Lone Walentin, Thies, Jenny, Emslie, Frances, Willemsen, Marjolein, Kleefstra, Tjitske, Pfundt, Rolf, Barrick, Rebekah, Chang, Richard, Loong, Lucy, Alfadhel, Majid, van der Smagt, Jasper, Nizon, Mathilde, Kurian, Manju A., Scott, Daniel J., Ziarek, Joshua J., Gordon, Sarah L., Baker, Kate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986325/
https://www.ncbi.nlm.nih.gov/pubmed/35101335
http://dx.doi.org/10.1016/j.gim.2021.12.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986325/
https://www.ncbi.nlm.nih.gov/pubmed/35101335
http://dx.doi.org/10.1016/j.gim.2021.12.002

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