Association of Monoamine Oxidase A (MAOA) Gene uVNTR and rs6323 Polymorphisms with Attention Deficit and Hyperactivity Disorder in Korean Children

Objective: Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder. The genetic cause of ADHD is still unclear, but the dopaminergic, serotonergic, and noradrenergic pathways have shown a strong association. In particular, monoamine oxidase A (MAOA) plays an important...

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Detalles Bibliográficos
Autores principales: Hwang, In Wook, Lim, Myung Ho, Kwon, Ho Jang, Jin, Han Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122096/
https://www.ncbi.nlm.nih.gov/pubmed/30344263
http://dx.doi.org/10.3390/medicina54030032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122096/
https://www.ncbi.nlm.nih.gov/pubmed/30344263
http://dx.doi.org/10.3390/medicina54030032

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