Chunk #10 — Introduction

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

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Based on the inversion, inv(3)(p21 : q24), that cosegregates with an AD/HD-like phenotype in a family and the other supportive studies described above, we selected DOCK3 and SLC9A9 as candidates to be evaluated in a family-based AD/HD genetic association study.