Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
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| Description | scientific article |
| Author/s |
author: Per Hoffmann Michael C O'Donovan Silvia Paracchini Roel Ophoff Fritz Poustka Markus M Nöthen Denise Harold Kerstin U. Ludwig Panos Deloukas Anthony Monaco Gerd Schulte-Körne Alistair T Pagnamenta |
| Publication date | March 26, 2010 |
| Language | English |
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