Primary hypoparathyroidism and multiple neuraxial involvement in mitochondrial disorder due to the variant m.15043G>A in MT-CYB

J Neurol Sci. 2020 Jul 15:414:116853. doi: 10.1016/j.jns.2020.116853. Epub 2020 Apr 18.
No abstract available

Keywords: Hereditary; Hypoparathyroidism; Lactic acidosis; Mitochondrial; Movement disorder; Multisystem disease; mtDNA.

Publication types

  • Letter

MeSH terms

  • DNA, Mitochondrial
  • Humans
  • Hypoparathyroidism* / complications
  • Hypoparathyroidism* / genetics
  • Mitochondrial Diseases* / genetics

Substances

  • DNA, Mitochondrial