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...

Бүрэн тодорхойлолт

Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид: Vernes, S, MacDermot, K, Monaco, A, Fisher, S
Бусад зохиолчид: European Society of Human Genetics
Формат: Journal article
Хэл сонгох:English
Хэвлэсэн: Macmillan Publishers Ltd. 2009
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