Login / Signup

Genetic change investigation in DOCK1 gene in an Iranian family with sign and symptoms of temporomandibular joint disorder (TMD).

Shamsoulmolouk NajafiFeyzollah Hashemi-GorjiHassan RoudgariMina GoudarziAmir Mohammad JafarzadeganNafiseh Sheykhbahaei
Published in: Clinical oral investigations (2024)
The role of genetic factors in the development of TMD has been described. The present study identified a nonsynonymous variant of the DOCK1 gene as a candidate for TMD and skeletal class III malocclusion in affected individuals in the Iranian pedigree.
Keyphrases
  • genome wide
  • copy number
  • dna methylation
  • genome wide identification
  • transcription factor