Genotypic and Haplotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Gene Polymorphisms with Particular Clinical Symptoms in Schizophrenia

Catechol-O-methyl transferase (COMT) gene variants are involved in different neuropsychiatric disorders and cognitive impairments, associated with altered dopamine function. This study investigated the genotypic and haplotypic association of COMT rs4680 and rs4618 polymorphisms with the severity of...

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Detalles Bibliográficos
Autores principales: Sagud, Marina, Tudor, Lucija, Nedic Erjavec, Gordana, Nikolac Perkovic, Matea, Uzun, Suzana, Mimica, Ninoslav, Madzarac, Zoran, Zivkovic, Maja, Kozumplik, Oliver, Konjevod, Marcela, Svob Strac, Dubravka, Pivac, Nela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379812/
https://www.ncbi.nlm.nih.gov/pubmed/37510262
http://dx.doi.org/10.3390/genes14071358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379812/
https://www.ncbi.nlm.nih.gov/pubmed/37510262
http://dx.doi.org/10.3390/genes14071358

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