Nonsense mutation in DEPDC5 gene in a patient with carbamazepine-responsive focal epilepsy-Reference-Cited by-同舟云学术

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Nonsense mutation in DEPDC5 gene in a patient with carbamazepine-responsive focal epilepsy

Published:2024 Issue: Volume:27 Page:100683
ISSN:2589-9864
Container-title:Epilepsy & Behavior Reports
language:en
Short-container-title:Epilepsy & Behavior Reports

Author:

Mulkerrin Grainne,Hennessy Michael J.

Publisher

Elsevier BV

Reference21 articles.

1. Localisation in focal epilepsy: a practical guide;Chowdhury;Pract Neurol,2021

2. Genetics of nonlesional focal epilepsy in adults and surgical implications;Karge;Clinical Epileptology,2023

3. Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder;Scheffer;Brain,1995

4. A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy;Steinlein;Nat Genet,1995

5. Sodium-channel defects in benign familial neonatal-infantile seizures;Heron;Lancet,2002

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