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Large Interruptions of GAA Repeat Expansion Mutations in Friedreich Ataxia Are Very Rare

  • Published:2018-11-21 Issue: Volume:12 Page:
  • ISSN:1662-5102
  • Container-title:Frontiers in Cellular Neuroscience
  • language:
  • Short-container-title:Front. Cell. Neurosci.

Author:

Al-Mahdawi Sahar,Ging Heather,Bayot Aurelien,Cavalcanti Francesca,La Cognata Valentina,Cavallaro Sebastiano,Giunti Paola,Pook Mark A.

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

Cited by 21 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. The Regulation of the Disease-Causing Gene FXN;Cells;2024-06-15

2. Etiology of Ataxia: A Mechanistic Insight of Autoimmune, Toxicity, and Genetic Approach;Mechanism and Genetic Susceptibility of Neurological Disorders;2024

3. A wearable motion capture suit and machine learning predict disease progression in Friedreich’s ataxia;Nature Medicine;2023-01

4. Neurogenetic motor disorders;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023

5. Replication dependent and independent mechanisms of GAA repeat instability;DNA Repair;2022-10
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