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Novel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy

  • Published:2019-01-30 Issue:1 Volume:12 Page:63-65
  • ISSN:2005-940X
  • Container-title:Journal of Movement Disorders
  • language:en
  • Short-container-title:JMD

Author:

Yoon So Hoon,Kim Nan Young,Kim Yun Joong,Lyoo Chul Hyoung

Funder

National Research Foundation of Korea

Ministry of Science, ICT and Future Planning

Publisher

The Korean Movement Disorder Society

Subject

Neurology (clinical),Neurology

Cited by 6 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. Transcriptome Profile in the Mouse Brain of Hepatic Encephalopathy and Alzheimer’s Disease;International Journal of Molecular Sciences;2022-12-30

2. Pathogenic mechanism and modeling of neuroferritinopathy;Cellular and Molecular Life Sciences;2021-01-13

3. Iron Metabolism and Related Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021

4. Brain MRI Pattern Recognition in Neurodegeneration With Brain Iron Accumulation;Frontiers in Neurology;2020-09-10

5. A Patient with Neuroferritinopathy Presenting with Juvenile-Onset Voice Tremor;Journal of Movement Disorders;2020-01-31
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