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- Title
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.
- Authors
de Silva, M G; Elliott, K; Dahl, H-H; Fitzpatrick, E; Wilcox, S; Delatycki, M; Williamson, R; Efron, D; Lynch, M; Forrest, S
- Abstract
Attention deficit hyperactivity disorder (ADHD) is a complex condition with high heritability. However, both biochemical investigations and association and linkage studies have failed to define fully the underlying genetic factors associated with ADHD. We have identified a family co-segregating an early onset behavioural/developmental condition, with features of ADHD and intellectual disability, with a pericentric inversion of chromosome 3, 46N inv(3)(p14:q21).
- Publication
Journal of medical genetics, 2003, Vol 40, Issue 10, p733
- ISSN
1468-6244
- Publication type
Journal Article
- DOI
10.1136/jmg.40.10.733