A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

Genetic investigations of people with impaired development of spoken language provide windows into key aspects of human biology. Over 15 years after FOXP2 was identified, most speech and language impairments remain unexplained at the molecular level. We sequenced whole genomes of nineteen unrelated...

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Detalles Bibliográficos
Autores principales: Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T., Shriberg, Lawrence D., Fisher, Simon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756287/
https://www.ncbi.nlm.nih.gov/pubmed/29463886
http://dx.doi.org/10.1038/s41380-018-0020-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756287/
https://www.ncbi.nlm.nih.gov/pubmed/29463886
http://dx.doi.org/10.1038/s41380-018-0020-x

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