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A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencing.

Alessia AzzaràIlaria CassanoCarla LintasLaura BernardiniFabio PilatoFioravante CaponeVincenzo Di LazzaroFiorella Gurrieri
Published in: European journal of neurology (2023)
These findings suggest that TRPM8 could be a new causative gene further linking migraine and recurrent facial palsy.
Keyphrases
  • copy number
  • genome wide
  • genome wide identification
  • soft tissue
  • gene expression
  • dna methylation
  • transcription factor