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

Heterozygous mutations in FOXP2, which encodes a forkhead transcription factor, have been shown to cause developmental verbal dyspraxia and language impairment. FOXP2 and its closest homolog, FOXP1, are coexpressed in brain regions that are important for language and cooperatively regulate developme...

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Hlavní autoři: Hamdan, Fadi F., Daoud, Hussein, Rochefort, Daniel, Piton, Amélie, Gauthier, Julie, Langlois, Mathieu, Foomani, Gila, Dobrzeniecka, Sylvia, Krebs, Marie-Odile, Joober, Ridha, Lafrenière, Ronald G., Lacaille, Jean-Claude, Mottron, Laurent, Drapeau, Pierre, Beauchamp, Miriam H., Phillips, Michael S., Fombonne, Eric, Rouleau, Guy A., Michaud, Jacques L.
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2010
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2978954/
https://ncbi.nlm.nih.gov/pubmed/20950788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2010.09.017
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