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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Pubblicato in:Mol Genet Genomic Med
Autori principali: Acosta, Maria T., Swanson, James, Stehli, Annamarie, Molina, Brooke S. G., Martinez, Ariel F., Arcos‐Burgos, Mauricio, Muenke, Maximilian
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2016
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Original Articles
Accesso online: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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