| Literature DB >> 32828702 |
Sophie Imhof1, Tomislav Kokotović2, Vanja Nagy3.
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.Entities:
Keywords: Mendelian disorders; PRDM12; congenital insensitivity to pain; nociception
Mesh:
Substances:
Year: 2020 PMID: 32828702 DOI: 10.1016/j.molmed.2020.07.007
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951