Varaico: Literature-Extracted Genetic Variants

Gene:SCN1A
Variant:p.L263Q
Back to variants list

SCN1A

NM_001165963.4:p.L263Q

Associated Papers

Epilepsy and Migraine Shared Genetic and Molecular Mechanisms: Focus on Therapeutic Strategies.

Gotra P et al.

Molecular Neurobiology, 2021

Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA.

Bertelli S et al.

Cephalalgia : an International Journal of Headache, 2019

Epilepsy and migraine-Are they comorbidity?

Liao J et al.

Genes & Diseases, 2018

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

Fan C et al.

Cephalalgia : an International Journal of Headache, 2016

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."