Orphanet: Hereditary neuropathy and spastic paraplegia: new mechanisms, biomarkers and treatment
x

Search for a research project

* (*) mandatory field

Hereditary neuropathy and spastic paraplegia: new mechanisms, biomarkers and treatment

    • Type of research project :
      • In vitro functional study
  • Website
    • Funding body(ies) :
      • ACADEMY OF FINLAND

Download more information on this project

  • Investigator of research project

  • Dr Emil YLIKALLIO
  • Stem Cells and Metabolism Research Program
  • University of Helsinki
  • Haartmaninkatu 8
  • 00290 HELSINKI
  • FINLAND
  • More information
  • Phone  : 358 503708976
  • Fax  : -
  • Website
Last update: May 2019

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.