Uncovering the missing mutations in pain
- PMID: 39159470
- DOI: 10.1097/j.pain.0000000000003253
Uncovering the missing mutations in pain
References
-
- Altassan R, Saud HA, Masoodi TA, Dosssari HA, Khalifa O, Al-Zaidan H, Sakati N, Rhabeeni Z, Al-Hassnan Z, Binamer Y, Alhashemi N, Wade W, Al-Zayed Z, Al-Sayed M, Al-Muhaizea MA, Meyer B, Al-Owain M, Wakil SM. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype. Am J Med Genet A 2017;173:1009–16.
-
- Barbacid M. Structural and functional properties of the TRK family of neurotrophin receptors. Ann N Y Acad Sci 1995;766:442–58.
-
- Daneshjou K, Jafarieh H, Raaeskarami SR. Congenital insensitivity to pain and anhydrosis (CIPA) syndrome: a report of 4 cases. Iran J Pediatr 2012;22:412–6.
-
- Dearborn GvN. A case of congenital general pure analgesia. J Nervous Ment Dis 1932;75:612–5.
-
- Indo Y, Tsuruta M, Hayashida Y, Karim MA, Ohta K, Kawano T, Mitsubuchi H, Tonoki H, Awaya Y, Matsuda I. Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis. Nat Genet 1996;13:485–8.
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