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...

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Detalles Bibliográficos
Autores principales: Vernes, Sonja C, MacDermot, Kay D, Monaco, Anthony P, Fisher, Simon E
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784575/
https://www.ncbi.nlm.nih.gov/pubmed/19352412
http://dx.doi.org/10.1038/ejhg.2009.43

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784575/
https://www.ncbi.nlm.nih.gov/pubmed/19352412
http://dx.doi.org/10.1038/ejhg.2009.43

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