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A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.
Kremeyer B, Lopera F, Cox JJ, Momin A, Rugiero F, Marsh S, Woods CG, Jones NG, Paterson KJ, Fricker FR, Villegas A, Acosta N, Pineda-Trujillo NG, Ramírez JD, Zea J, Burley MW, Bedoya G, Bennett DL, Wood JN, Ruiz-Linares A. Kremeyer B, et al. Among authors: momin a. Neuron. 2010 Jun 10;66(5):671-80. doi: 10.1016/j.neuron.2010.04.030. Neuron. 2010. PMID: 20547126 Free PMC article.
Pain channelopathies.
Cregg R, Momin A, Rugiero F, Wood JN, Zhao J. Cregg R, et al. Among authors: momin a. J Physiol. 2010 Jun 1;588(Pt 11):1897-904. doi: 10.1113/jphysiol.2010.187807. Epub 2010 Feb 8. J Physiol. 2010. PMID: 20142270 Free PMC article. Review.
Persistent pain: the contribution of Na(V)1.9.
Smith ES, Momin A. Smith ES, et al. Among authors: momin a. J Physiol. 2008 May 1;586(9):2249-50. doi: 10.1113/jphysiol.2008.152520. Epub 2008 Mar 6. J Physiol. 2008. PMID: 18325975 Free PMC article. No abstract available.
176 results