A POLG2 Homozygous Mutation in an Autosomal Recessive Epilepsy Family Without Ophthalmoplegia-Reference-Cited by-同舟云学术

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A POLG2 Homozygous Mutation in an Autosomal Recessive Epilepsy Family Without Ophthalmoplegia

Published:2019 Issue:3 Volume:15 Page:418
ISSN:1738-6586
Container-title:Journal of Clinical Neurology
language:en
Short-container-title:J Clin Neurol

Author:

Lee Su Jeong¹,Kanwal Sumaira²,Yoo Da Hye¹,Park Hye Ri¹,Choi Byung-Ok³,Chung Ki Wha¹

Affiliation:

1. Department of Biological Sciences, Kongju National University, Gongju, Korea.

2. Department of Biosciences, COMSATS University Islamabad, Sahiwal, Pakistan.

3. Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Funder

National Research Foundation of Korea

Publisher

Korean Neurological Association

Subject

Neurology (clinical),Neurology

Link

https://synapse.koreamed.org/pdf/10.3988/jcn.2019.15.3.418

Cited by 4 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. POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the Literature;The Cerebellum;2023-04-22

2. Targeting Staufen 1 with antisense oligonucleotides for treating ALS and SCA2;2022-11-17

3. Multisystem presentation of a homozygous POLG2 variant;European Journal of Medical Genetics;2020-05

4. Answer to Finsterer about “Multisystem presentation of a homozygous POLG2 variant”;European Journal of Medical Genetics;2020-05

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