Lataa...
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...
Tallennettuna:
| Julkaisussa: | Mol Genet Genomic Med |
|---|---|
| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2016
|
| Aiheet: | |
| Linkit: | 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 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|