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Article

Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.

Psychiatric genetics - 1 Apr 2010

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

Abstract excerpt

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, resp...

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Source

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Identifiers

PMID: 20032819
DOI: 10.1097/YPG.0b013e3283351209
PMCID: PMC3085270

Genes

DOCK3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20032819-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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