Current knowledge of SLC6A1-related neurodevelopmental disorders

Advances in gene discovery have identified genetic variants in the solute carrier family 6 member 1 gene as a monogenic cause of neurodevelopmental disorders, including epilepsy with myoclonic atonic seizures, autism spectrum disorder and intellectual disability. The solute carrier family 6 member 1...

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Detalles Bibliográficos
Autores principales: Goodspeed, Kimberly, Pérez-Palma, Eduardo, Iqbal, Sumaiya, Cooper, Dominique, Scimemi, Annalisa, Johannesen, Katrine M, Stefanski, Arthur, Demarest, Scott, Helbig, Katherine L, Kang, Jingqiong, Shaffo, Frances C, Prentice, Brandon, Brownstein, Catherine A, Lim, Byungchan, Helbig, Ingo, De Los Reyes, Emily, McKnight, Dianalee, Crunelli, Vincenzo, Campbell, Arthur J, Møller, Rikke S, Freed, Amber, Lal, Dennis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677605/
https://www.ncbi.nlm.nih.gov/pubmed/33241211
http://dx.doi.org/10.1093/braincomms/fcaa170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677605/
https://www.ncbi.nlm.nih.gov/pubmed/33241211
http://dx.doi.org/10.1093/braincomms/fcaa170

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