A novel splicing variant in MICAL-1 gene is associated with epilepsy
Author:
Funder
National Natural Science Foundation of China
Health Commission of Henan Province
Natural Science Foundation of Hunan Province
Publisher
Elsevier BV
Reference13 articles.
1. Mutations in MICAL-1 cause autosomal-dominant lateral temporal epilepsy;Dazzo;Ann. Neurol.,2018
2. Benign epilepsy with centrotemporal spikes - current concepts of diagnosis and treatment;Dryzalowski;Neurol. Neurochir. Pol.,2018
3. DEPDC5 mutations in genetic focal epilepsies of childhood;Lal;Ann. Neurol.,2014
4. MICAL1 regulates actin cytoskeleton organization, directional cell migration and the growth of human breast cancer cells as orthotopic xenograft tumours;McGarry;Cancer Lett.,2021
5. Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families;Michelucci;Epilepsia,2003
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