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De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

✍ Scribed by Fadi F. Hamdan; Hussein Daoud; Daniel Rochefort; Amélie Piton; Julie Gauthier; Mathieu Langlois; Gila Foomani; Sylvia Dobrzeniecka; Marie-Odile Krebs; Ridha Joober; Ronald G. Lafrenière; Jean-Claude Lacaille; Laurent Mottron; Pierre Drapeau; Miriam H. Beauchamp; Michael S. Phillips; Eric Fombonne; Guy A. Rouleau; Jacques L. Michaud

Book ID: 113422930
Publisher: American Society of Human Genetics
Year: 2010
Tongue: English
Weight: 670 KB
Volume: 87
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2010.09.017

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