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Novel truncating germline variant reinforces TINF2 as a susceptibility gene for familial non-medullary thyroid cancer.

Josep OriolaOrland DíezMireia MoraIrene HalperinSandra MartínezMiriam MasasAnna TenesAnna BernalRafael DuranAida Orois
Published in: Journal of medical genetics (2024)
pathogenic variants appear to be a significant risk factor for the development of NMTC and/or melanoma.
Keyphrases
  • copy number
  • genome wide
  • early onset
  • dna repair
  • genome wide identification
  • dna methylation
  • gene expression
  • basal cell carcinoma