Novel and Novel De Novo Mutations in NTRK1 Associated With Congenital Insensitivity to Pain With Anhidrosis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference19 articles.
1. Congenital insensitivity to pain with anhydrosis. A unique syndrome in two male siblings.;Swanson;Arch Neurol,1963
2. Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis.;Indo;Clin Genet,2012
3. Mutations in the TRKANGF receptor gene in patients with congenital insensitivity to pain with anhidrosis.;Indo;Nat Genet,1996
4. Mechanisms of disease in hereditary sensory and autonomic neuropathies.;Rotthier;Nat Rev Neurol,2012
5. Severe sensory and sympathetic neuropathies in mice carrying a disrupted TrkNGF receptor gene.;Smeyne;Nature,1994
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2. Structural analysis of TrkA mutations in patients with congenital insensitivity to pain reveals PLCγ as an analgesic drug target;Science Signaling;2022-04-26
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4. Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation;European Journal of Medical Genetics;2020-01
5. Congenital Loss of Permanent Teeth in a Patient With Congenital Insensitivity to Pain With Anhidrosis due to 2 Novel Mutations in the NTRK1 Gene;Journal of Oral and Maxillofacial Surgery;2018-12
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