Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus control groups (1.41-fold, p = 1.0 × 10(-5)) and an increase in affected subjec...
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Journal article |
Sprache: | English |
Veröffentlicht: |
2014
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