Pain: New familial pain syndrome caused by TRPA1 mutation

Nature Reviews Neurology

Volumn 6, Issue 8, 2010, Pages 412-

  Wood, Heather ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

TRANSIENT RECEPTOR POTENTIAL CHANNEL;

ARTICLE; COLOMBIAN; ETHNIC GROUP; FAMILIAL DISEASE; FAMILIAL EPISODIC PAIN SYNDROME; GENE; GENE FUNCTION; GENE MUTATION; HUMAN; MULTIGENE FAMILY; NONHUMAN; PAIN; PATHOGENESIS; PRIORITY JOURNAL; TRPA1 GENE;

EID: 77956256392     PISSN: 17594758     EISSN: 17594766     Source Type: Journal    
DOI: 10.1038/nrneurol.2010.97     Document Type: Article

References (1)

1. Kremeyer, B. et al. A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron 66, 671-680 (2010)