A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia

J Genet Genomics. 2021 Aug 20;48(8):751-754. doi: 10.1016/j.jgg.2021.06.008. Epub 2021 Jul 7.
No abstract available

Publication types

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

MeSH terms

  • Spastic Paraplegia, Hereditary*