Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

Neurodevelopmental disorders that disturb speech and language are highly heritable. Isolation of the underlying genetic risk factors has been hampered by complexity of the phenotype and potentially large number of contributing genes. One exception is the identification of rare heterozygous mutations...

詳細記述

書誌詳細
主要な著者: Vernes, S, MacDermot, K, Monaco, A, Fisher, S
その他の著者: European Society of Human Genetics
フォーマット: Journal article
言語:English
出版事項: Macmillan Publishers Ltd. 2009
主題: