PRDM12: New Opportunity in Pain Research. Review uri icon

Overview

abstract

  • PRDM12 is a newly identified causative gene for a type of congenital insensitivity to pain disorder, which is characterized by the inability to perceive pain. Here, we discuss the (patho)physiology of PRDM12 function and the opportunities and challenges those data provide for novel therapeutic approaches in various pain disorders.

publication date

  • August 20, 2020

Research

keywords

  • Carrier Proteins
  • Nerve Tissue Proteins
  • Pain

Identity

Scopus Document Identifier

  • 85089688711

Digital Object Identifier (DOI)

  • 10.1016/j.molmed.2020.07.007

PubMed ID

  • 32828702

Additional Document Info

volume

  • 26

issue

  • 10