Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes

INTRODUCTION: Autism spectrum disorder is a genetically and phenotypically heterogeneous group. Genetic studies carried out to date have suggested that both common and rare genetic variants play a role in the etiology of this disorder. In our study, we aimed to investigate the effect of FOXP2, GRIN2...

Descripción completa

Detalles Bibliográficos
Autores principales: YALÇINTEPE, Sinem, GÖRKER, Işık, DEMİR, Selma, ATLI, Emine İkbal, ATLI, Engin, TOZKIR, Hilmi, SÜT, Necdet, ÖZEN, Yasemin, EKER, Damla, MAİL, Çisem, GÜLER, Hazal SEZGİNER, ZHURI, Drenushe, GURKAN, Hakan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Noro-Psikiyatri Arsivi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419723/
https://www.ncbi.nlm.nih.gov/pubmed/34526837
http://dx.doi.org/10.29399/npa.27407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419723/
https://www.ncbi.nlm.nih.gov/pubmed/34526837
http://dx.doi.org/10.29399/npa.27407

Ejemplares similares