De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
- 14 October 2010
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 87 (5), 671-678
- https://doi.org/10.1016/j.ajhg.2010.09.017
Abstract
No abstract availableThis publication has 36 references indexed in Scilit:
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