A novel loss-of-function compound heterozygous mutation of MYORG causes idiopathic basal ganglia calcification 7

Parkinsonism Relat Disord. 2022 Apr:97:65-67. doi: 10.1016/j.parkreldis.2022.03.011. Epub 2022 Mar 21.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basal Ganglia / diagnostic imaging
  • Basal Ganglia Diseases* / diagnostic imaging
  • Basal Ganglia Diseases* / genetics
  • Calcinosis* / genetics
  • Humans
  • Mutation / genetics
  • Pedigree
  • Sodium-Phosphate Cotransporter Proteins, Type III / genetics

Substances

  • Sodium-Phosphate Cotransporter Proteins, Type III