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Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

AuthorsKathrin Müller, Peter M Andersen, Annemarie Hübers, Nicolai Marroquin, Alexander E Volk, Karin M Danzer, Thomas Meitinger, Albert C Ludolph, Tim M Strom, Jochen H Weishaupt
JournalBrain : a journal of neurology (Brain) Vol. 137 Issue Pt 12 Pg. e309 (Dec 2014) ISSN: 1460-2156 [Electronic] England
PMID25113787 (Publication Type: Letter, Research Support, Non-U.S. Gov't, Comment)
Chemical References
  • DNA, Mitochondrial
  • Mitochondrial Proteins
Topics
  • Amyotrophic Lateral Sclerosis (etiology)
  • DNA, Mitochondrial (genetics)
  • Female
  • Frontotemporal Dementia (etiology)
  • Humans
  • Male
  • Mitochondria (pathology)
  • Mitochondrial Diseases (complications)
  • Mitochondrial Proteins (genetics)

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