ADGRL3 (LPHN3) variants are associated with a refined phenotype of ADHD in the MTA study

BACKGROUND: ADHD is the most common neuropsychiatric condition affecting individuals of all ages. Long‐term outcomes of affected individuals and association with severe comorbidities as SUD or conduct disorders are the main concern. Genetic associations have been extensively described. Multiple stud...

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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: Acosta, Maria T., Swanson, James, Stehli, Annamarie, Molina, Brooke S. G., Martinez, Ariel F., Arcos‐Burgos, Mauricio, Muenke, Maximilian
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2016
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5023939/
https://ncbi.nlm.nih.gov/pubmed/27652281
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.230
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