A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Brain. 2015 Sep;138(Pt 9):e376. doi: 10.1093/brain/awv014. Epub 2015 Feb 12.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Amyotrophic Lateral Sclerosis / etiology*
  • DNA, Mitochondrial / genetics*
  • Female
  • Frontotemporal Dementia / etiology*
  • Humans
  • Male
  • Mitochondria / pathology*
  • Mitochondrial Diseases / complications*
  • Mitochondrial Proteins / genetics*

Substances

  • DNA, Mitochondrial
  • Mitochondrial Proteins