SCN1A c.788T>A ;(p.L263Q)

Variant ID: 2-166908405-A-T

NM_001165963.1(SCN1A):c.788T>A;(p.L263Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Epilepsy and migraine-Are they comorbidity?

Genes & Diseases
Liao, Jin J; Tian, Xin X; Wang, Hao H; Xiao, Zheng Z
Publication Date: 2018-06

Variant appearance in text: SCN1A: L263Q
PubMed Link: 30258939
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.

Cephalalgia : An International Journal Of Headache
Fan, Chunxiang C; Wolking, Stefan S; Lehmann-Horn, Frank F; Hedrich, Ulrike Bs UB; Freilinger, Tobias T; Lerche, Holger H; Borck, Guntram G; Kubisch, Christian C; Jurkat-Rott, Karin K
Publication Date: 2016-11

Variant appearance in text: SCN1A: L263Q
PubMed Link: 26763045
Variant Present in the following documents:
  • Main text
  • 10.1177_0333102415608360.pdf
View BVdb publication page