Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases-Reference-Cited by-同舟云学术

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Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases

Published:2014-08-01 Issue:11 Volume:83 Page:1018-1021
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Bagnall R. D.,Crompton D. E.,Cutmore C.,Regan B. M.,Berkovic S. F.,Scheffer I. E.,Semsarian C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 19 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. Genetics and SUDEP: Challenges and Future Directions;Seizure: European Journal of Epilepsy;2023-08

2. ILAE Genetic Literacy Series: Postmortem Genetic Testing in Sudden Unexpected Death in Epilepsy;Epileptic Disorders;2023-07-04

3. Update on Sudden Unexpected Death in Epilepsy;Neurologic Clinics;2022-11

4. Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death;PLOS ONE;2022-04-29

5. SUDEP risk and autonomic dysfunction in genetic epilepsies;Autonomic Neuroscience;2022-01

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