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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Main Authors: Markunas, Christina A., Quinn, Kaia S., Collins, Ann L., Garrett, Melanie E., Lachiewicz, Ave M., Sommer, Jennifer L., Morrissey-Kane, Erin, Kollins, Scott H., Anastopoulos, Arthur D., Ashley-Koch, Allison E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha: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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