Functional investigation of microRNA pathways in human speech and language disorders
<p>The forkhead-box protein P2 (FOXP2) is a transcription factor implicated in an inherited human speech and language disorder. A heterozygous R553H mutation in the gene is associated with a monogenic form of developmental verbal dyspraxia. Reduced functional dosage in mice brains causes alter...
| Main Author: | |
|---|---|
| Other Authors: | |
| Format: | Thesis |
| Language: | English |
| Published: |
2014
|
| Subjects: |