A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.

Human monogenic pain syndromes have provided important insights into the molecular mechanisms that underlie normal and pathological pain states. We describe an autosomal-dominant familial episodic pain syndrome characterized by episodes of debilitating upper body pain, triggered by fasting and physi...

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Bibliographic Details
Main Authors:	Kremeyer, B, Lopera, F, Cox, J, Momin, A, Rugiero, F, Marsh, S, Woods, C, Jones, N, Paterson, K, Fricker, F, Villegas, A, Acosta, N, Pineda-Trujillo, N, Ramírez, J, Zea, J, Burley, M, Bedoya, G, Bennett, D, Wood, J, Ruiz-Linares, A
Format:	Journal article
Language:	English
Published:	2010

A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.

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