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...

Mô tả đầy đủ

Chi tiết về thư mục
Những tác giả chính: Vernes, S, MacDermot, K, Monaco, A, Fisher, S
Tác giả khác: European Society of Human Genetics
Định dạng: Journal article
Ngôn ngữ:English
Được phát hành: Macmillan Publishers Ltd. 2009
Những chủ đề: