KCNH2 Gene Mutation: A Potential Link Between Epilepsy and Long QT-2 Syndrome-Reference-Cited by-同舟云学术

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KCNH2 Gene Mutation: A Potential Link Between Epilepsy and Long QT-2 Syndrome

Published:2012-04-19 Issue:3-4 Volume:26 Page:382-386
ISSN:0167-7063
Container-title:Journal of Neurogenetics
language:en
Short-container-title:Journal of Neurogenetics

Author:

Zamorano-León José J.¹,Yañez Rosa²,Jaime Gabriel³,Rodriguez-Sierra Pablo¹,Calatrava-Ledrado Laura¹,Alvarez-Granada Roman R.⁴,Mateos-Cáceres Petra Jiménez¹,Macaya Carlos¹,López-Farré Antonio J.¹

Affiliation:

1. Cardiovascular Research Unit of the Cardiology Department, Cardiovascular Institute, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain

2. Neurology Department

3. Clinic Analysis Department

4. Intensive Medicine Department of Hospital Cristal Piñor, Complexo Hospitalario de Ourense, Ourense, Spain

Publisher

Informa UK Limited

Subject

Cellular and Molecular Neuroscience,Genetics

Link

https://www.tandfonline.com/doi/pdf/10.3109/01677063.2012.674993

Reference24 articles.

1. New SCN5A mutation in a SUDEP victim with idiopathic epilepsy

2. Guidelines for Epidemiologic Studies on Epilepsy. Commission on Epidemiology and Prognosis, International League Against Epilepsy

3. Congenital long QT syndrome

4. Do Glia Have Heart? Expression and Functional Role forEther-A-Go-GoCurrents in Hippocampal Astrocytes

5. Kv1.1 Potassium Channel Deficiency Reveals Brain-Driven Cardiac Dysfunction as a Candidate Mechanism for Sudden Unexplained Death in Epilepsy

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1. Sudden unexpected death in epilepsy: respiratory vs. cardiac contributions;Cardiovascular Research;2024-08-07

2. Neurocardiac pathologies associated with potassium channelopathies;Epilepsia;2024-08

3. An intracellular hydrophobic nexus critical for hERG1 channel slow deactivation;Biophysical Journal;2024-07

4. Generation of KCNH2 heterozygous knockout induced pluripotent stem cell (iPSC) line (Long and Short QT Syndrome);Stem Cell Research;2024-06

5. Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome;PLOS ONE;2024-01-05

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