Article info

Download PDFPDF
Original research
A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia

Authors

  1. Correspondence to Dr Eran Cohen-Barak, Emek Medical Center, Afula 1834111, Israel; erancb79{at}gmail.com
View Full Text

Citation

Cohen-Barak E, Danial-Farran N, Chervinsky E, et al
A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia

Publication history

  • Received March 3, 2022
  • Accepted June 7, 2022
  • First published June 16, 2022.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.