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Genetic variants in SLC9A9 are associated with measures of Attention-deficit/hyperactivity disorder symptoms in families
OBJECTIVE: A family was previously identified that cosegregates a pericentric inversion, inv(3)(p14 : q21), with an early-onset developmental condition, characterized by impulsive behavior and intellectual deficit. The inversion breakpoints lie within DOCK3 and SLC9A9 at the p-arm and q-arm, respect...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3085270/ https://ncbi.nlm.nih.gov/pubmed/20032819 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/YPG.0b013e3283351209 |
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