A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions-Reference-Cited by-同舟云学术

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A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions

Published:2002-07-01 Issue:7 Volume:59 Page:1137
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Kananura Colette,Haug Karsten,Sander Thomas,Runge Uwe,Gu Wenli,Hallmann Kerstin,Rebstock Johannes,Heils Armin,Steinlein Ortrud K.

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 240 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unraveling the genetic basis of epilepsy: Recent advances and implications for diagnosis and treatment;Brain Research;2024-11

2. GABA(A) Receptor Subunit (γ2, δ, β1-3) Variants in Genetic Epilepsy: A Comprehensive Summary of 206 Clinical Cases;Journal of Child Neurology;2024-09-03

3. GABRG2 mutations in genetic epilepsy with febrile seizures plus: structure, roles, and molecular genetics;Journal of Translational Medicine;2024-08-14

4. Established and emerging GABAA receptor pharmacotherapy for epilepsy;Frontiers in Pharmacology;2024-02-21

5. GABA_A receptors in epilepsy: Elucidating phenotypic divergence through functional analysis of genetic variants;Journal of Neurochemistry;2023-08-24

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