A Functional Genetic Link between Distinct Developmental Language Disorders

BACKGROUND: Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and language disorder. We hypothesized that neural pathways downstream of FOXP2 influence more common phenotypes, such as specific language impairment. METHODS: We performed genomic screening for regions bou...

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Detaylı Bibliyografya
Asıl Yazarlar: Vernes, Sonja C., Newbury, Dianne F., Abrahams, Brett S., Winchester, Laura, Nicod, Jérôme, Groszer, Matthias, Alarcón, Maricela, Oliver, Peter L., Davies, Kay E., Geschwind, Daniel H., Monaco, Anthony P., Fisher, Simon E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2756409/
https://ncbi.nlm.nih.gov/pubmed/18987363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1056/NEJMoa0802828
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