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Paper Details

A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.
Neuron
313
2010
25 cM region, Human, N855S, TRPA1, TRPA1 gene, autosomal-dominant familial episodic pain syndrome, chromosome 8q12-8q13, debilitating upper body pain, familial episodic pain syndrome, humans, monogenic pain syndromes, mustard
Author NameAffiliation
Barbara KremeyerUniversity College London
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Release 1.2