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High intra-familiar clinical variability in MORC2 mutated CMT2 patients

  • Published:2017-02-23 Issue:4 Volume:140 Page:e21-e21
  • ISSN:0006-8950
  • Container-title:Brain
  • language:en
  • Short-container-title:

Author:

Semplicini Claudio,Ollagnon-Roman Elisabeth,Leonard-Louis Sarah,Piguet-Lacroix Guenaelle,Silvestre Manon,Latour Philippe,Stojkovic Tanya

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Reference9 articles.

1. MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs;Ann Neurol,2016

2. Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z with MORC2 mutations;Brain,2016

3. Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene;Brain,2016

4. The MORC family: new epigenetic regulators of transcription and DNA damage response;Epigenetics,2013

5. MORC2 signaling integrates phosphorylation-dependent, ATPase-coupled chromatin remodeling during the DNA damage response;Cell Rep,2012
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