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A Functional Genetic Link between Distinct Developmental Language Disorders
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New England, USA (NEJM): 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.
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content.nejm.org/cgi/content/short/359/22/2337
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