Epileptic Variants

Journal of Neurology, Neurosurgery and Psychiatry - United Kingdom
doi 10.1136/jnnp.s1-8.31.223
Full Text
Abstract

Available in full text

Date
Authors
Publisher

BMJ

Related search

Rare Copy Number Variants Are an Important Cause of Epileptic Encephalopathies

Annals of Neurology
Neurology
2011English

Epileptic Encephalopathy and Cerebellar Atrophy Resulting From Compound Heterozygous CACNA2D2 Variants

Case Reports in Genetics
2018English

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy With Contractures, Macrocephaly, and Dyskinesias

American Journal of Human Genetics
Genetics
2019English

Re-Annotation of 191 Developmental and Epileptic Encephalopathy-Associated Genes Unmasks De Novo Variants in SCN1A

npj Genomic Medicine
GeneticsMolecular Biology
2019English

Epileptic Encephalopathy

Journal of Child Neurology
Child HealthNeurologyPediatricsPerinatology
2016English

Heterozygous RNF13 Gain-Of-Function Variants Are Associated With Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to Thrive

American Journal of Human Genetics
Genetics
2019English

Epileptic Asystole

European Neurology
Neurology
2010English

Infrequent Epileptic Fits

BMJ
1935English

Epileptic by David B.

A Moveable Type
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy