CNTNAP2 c.403-25138C>T

Variant ID: 7-146715861-C-T

NM_014141.5(CNTNAP2):c.403-25138C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Connection between genetic and clinical data in bipolar disorder.

Plos One
Mellerup, Erling E; Andreassen, Ole O; Bennike, Bente B; Dam, Henrik H; Djurovic, Srdjan S; Durovic, Srdjan S; Hansen, Thomas T; Melle, Ingrid I; Møller, Gert Lykke GL; Mors, Ole O; Koefoed, Pernille P
Publication Date: 2012

Variant appearance in text: rs1024676
PubMed Link: 23028568
Variant Present in the following documents:
  • Main text
  • pone.0044623.pdf
View BVdb publication page



CNTNAP2 variants affect early language development in the general population.

Genes, Brain, And Behavior
Whitehouse, A J O AJ; Bishop, D V M DV; Ang, Q W QW; Pennell, C E CE; Fisher, S E SE
Publication Date: 2011-06

Variant appearance in text: rs1024676
PubMed Link: 21310003
Variant Present in the following documents:
  • Main text
  • gbb0010-0451.pdf
View BVdb publication page



Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.

European Journal Of Human Genetics : Ejhg
Villanueva, Pia P; Newbury, Dianne F DF; Jara, Lilian L; De Barbieri, Zulema Z; Mirza, Ghazala G; Palomino, Hernán M HM; Fernández, María Angélica MA; Cazier, Jean-Baptiste JB; Monaco, Anthony P AP; Palomino, Hernán H
Publication Date: 2011-06

Variant appearance in text: rs1024676
PubMed Link: 21248734
Variant Present in the following documents:
  • Main text
View BVdb publication page