FOXP2 c.2003+2659C>G

Variant ID: 7-114307150-C-G

NM_014491.3(FOXP2):c.2003+2659C>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Journal Of Neurodevelopmental Disorders
Peter, Beate B; Raskind, Wendy H WH; Matsushita, Mark M; Lisowski, Mark M; Vu, Tiffany T; Berninger, Virginia W VW; Wijsman, Ellen M EM; Brkanac, Zoran Z
Publication Date: 2011-03

Variant appearance in text: rs12705970
PubMed Link: 21484596
Variant Present in the following documents:
  • Main text
  • 11689_2010_Article_9065.pdf
View BVdb publication page



Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.

Journal Of Neurodevelopmental Disorders
Rice, Mabel L ML; Smith, Shelley D SD; Gayán, Javier J
Publication Date: 2009-12

Variant appearance in text: rs12705970
PubMed Link: 19997522
Variant Present in the following documents:
  • Main text
  • 11689_2009_Article_9031.pdf
View BVdb publication page