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NaV1.8/NaV1.9 double deletion mildly affects acute pain responses in mice.
Pain. 2024 Oct 4. doi: 10.1097/j.pain.0000000000003411. Online ahead of print.
Pain. 2024.
PMID: 39382328
Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.
Kurth I, Baumgartner M, Schabhüttl M, Tomni C, Windhager R, Strom TM, Wieland T, Gremel K, Auer-Grumbach M.
Kurth I, et al. Among authors: tomni c.
Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):875-8. doi: 10.1002/ajmg.b.32458. Epub 2016 May 17.
Am J Med Genet B Neuropsychiatr Genet. 2016.
PMID: 27184211
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