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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...

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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

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