Advances on the Genetics of Mendelian Idiopathic Epilepsies
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry
Reference117 articles.
1. 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
2. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features;Kalachikov;Nat Genet,2002
3. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy;Morante-Redolat;Hum Mol Genet,2002
4. Genetics of epilepsy syndromes starting in the first year of life;Deprez;Neurology,2009
5. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns;Singh;Nat Genet,1998
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1. Clinical and genetic features of GATOR1 complex-associated epilepsy;Journal of Medical Genetics;2023-01-05
2. A Novel Mutation in KCDT7 Gene in an Indian Girl With Progressive Myoclonus Epilepsy;Cureus;2021-02-19
3. GABRG2 C588T gene polymorphisms might be a predictive genetic marker of febrile seizures and generalized recurrent seizures: a case-control study in a Romanian pediatric population;Archives of Medical Science;2018
4. Epilepsy and chromosome 18 abnormalities: A review;Seizure;2015-11
5. Advances on genetic rat models of epilepsy;Experimental Animals;2015
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