Communication deficits in a case of a deletion in 7q31.1-q31.33 encompassing FOXP2.
Copy number variants (CNVs) found in individuals with communication deficits provide a valuable window to the genetic causes of problems with language and, more generally, to the genetic foundation of the human-specific ability to learn and use languages. This paper reports on the language and commu...
| Published in: | Clinical Linguistics & Phonetics Vol. 37; no. 12; pp. 1157 - 1171 |
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| Main Authors: | , |
| Format: | case study pictorial tables/charts tracings Journal Article |
| Published: |
Taylor & Francis Ltd
2023
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| Online Access: | View this record in EBSCOhost |