Novel <b><i>KCNQ3</i></b> Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures-Reference-Cited by-同舟云学术

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Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures

Published:2016 Issue:4 Volume:7 Page:189-196
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Maljevic Snezana,Vejzovic Sabina,Bernhard Matthias K.,Bertsche Astrid,Weise Sebastian,Döcker Miriam,Lerche Holger,Lemke Johannes R.,Merkenschlager Andreas,Syrbe Steffen

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 20 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. Self-limited Familial Neonatal Epilepsy due to the c.1589G > A Novel Pathogenic Variant in KCNQ2: A Family Report;Journal of Pediatric Epilepsy;2023-07-28

2. Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes;Brain;2023-07-12

3. ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy;Epileptic Disorders;2023-06-22

4. A Review of Current and Prospective Treatments for Channelopathies, with a Focus on Gene and Protein Therapy;Current Pharmaceutical Design;2023-05

5. Aquatic Freshwater Vertebrate Models of Epilepsy Pathology: Past Discoveries and Future Directions for Therapeutic Discovery;International Journal of Molecular Sciences;2022-08-03

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