FOXP2 c.2003+5562G>T

Variant ID: 7-114310053-G-T

NM_014491.3(FOXP2):c.2003+5562G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Neuroimaging genetics studies of specific reading disability and developmental language disorder: A review.

Language And Linguistics Compass
Landi, Nicole N; Perdue, Meaghan M
Publication Date: 2019-09

Variant appearance in text: rs12705971
PubMed Link: 31844423
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

The Journal Of Neuroscience : The Official Journal Of The Society For Neuroscience
Pinel, Philippe P; Fauchereau, Fabien F; Moreno, Antonio A; Barbot, Alexis A; Lathrop, Mark M; Zelenika, Diana D; Le Bihan, Denis D; Poline, Jean-Baptiste JB; Bourgeron, Thomas T; Dehaene, Stanislas S
Publication Date: 2012-01-18

Variant appearance in text: rs12705971
PubMed Link: 22262880
Variant Present in the following documents:
  • Main text
View BVdb publication page