Investigating Sequence Variations in <i>CNTNAP2</i> and <i>SETBP1</i> Genes in Language Disorders
Homozygosity for <i>SETBP1</i> rs11082414 polymorphic variant increases language disorder susceptibility. This study underscores the genetic dimension of language disorder, urging physicians' awareness and early intervention strategies to mitigate its impact.
Authors
- Betül Turan (ORCID: https://orcid.org/0000-0003-0256-9981)
- Ayşe Gül Zamanı (ORCID: https://orcid.org/0000-0003-0329-9047)
- Emine Göktaş (ORCID: https://orcid.org/0000-0002-3635-8763)
- Necati Uzun (ORCID: https://orcid.org/0000-0003-3381-2331)
- Mahmut Selman Yıldırım (ORCID: https://orcid.org/0000-0002-3986-5517)
- Ayşegül Tuğba Hıra Selen (ORCID: https://orcid.org/0000-0003-1065-5548)
Institutions
- Necmettin Erbakan University (TR)
Publication Details
- Journal
- Clinical Psychopharmacology and Neuroscience
- Published
- 2024-10-14
- DOI
- https://doi.org/10.9758/cpn.24.1204
- Primary Topic
- Language Development and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Necmettin Erbakan Üniversitesi