Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:family
|
| gptkbp:disorderType |
developmental verbal dyspraxia
|
| gptkbp:heritability |
autosomal dominant
|
| https://www.w3.org/2000/01/rdf-schema#label |
KE family
|
| gptkbp:impact |
language comprehension
speech production orofacial motor control |
| gptkbp:location |
gptkb:London,_United_Kingdom
|
| gptkbp:mediaCoverage |
gptkb:BBC
gptkb:The_New_York_Times |
| gptkbp:mutationAssociatedWith |
gptkb:FOXP2_gene
|
| gptkbp:mutationDiscoveredBy |
Cecilia S. L. Lai
|
| gptkbp:mutationDiscoveredYear |
2001
|
| gptkbp:notableFor |
speech and language disorder
|
| gptkbp:numberOfMembers |
about 30
|
| gptkbp:relatedTo |
gptkb:FOXP2_gene
|
| gptkbp:studiedBy |
gptkb:Simon_E._Fisher
1990s Faraneh Vargha-Khadem |
| gptkbp:subjectOf |
numerous scientific studies
|
| gptkbp:bfsParent |
gptkb:FOXP2
|
| gptkbp:bfsLayer |
7
|