A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech de...
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
About this item
Full title
Author / Creator
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. and Fisher, Simon E.
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
Formats
Publication information
Publisher
London: Nature Publishing Group UK
Subjects
More information
Scope and Contents
Contents
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 individuals diagnosed with childhood apraxia...
Alternative Titles
Full title
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6756287
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6756287
Other Identifiers
ISSN
1359-4184
E-ISSN
1476-5578
DOI
10.1038/s41380-018-0020-x
