Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report

BACKGROUND: Mutations in voltage-gated sodium channel (SCN) genes are supposed to be of importance in the etiology of psychiatric and neurological diseases, in particular in the etiology of seizures. Previous studies report a potential susceptibility region at the chromosomal locus 2q including SCN1...

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Detalles Bibliográficos
Autores principales: Nickel, Kathrin, Tebartz van Elst, Ludger, Domschke, Katharina, Gläser, Birgitta, Stock, Friedrich, Endres, Dominique, Maier, Simon, Riedel, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090917/
https://www.ncbi.nlm.nih.gov/pubmed/30071822
http://dx.doi.org/10.1186/s12888-018-1822-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090917/
https://www.ncbi.nlm.nih.gov/pubmed/30071822
http://dx.doi.org/10.1186/s12888-018-1822-8

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