Sporadic onset of erythermalgia: A gain-of-function mutation in Nav1.7-Reference-Cited by-同舟云学术

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Sporadic onset of erythermalgia: A gain-of-function mutation in Nav1.7

Published:2006-03 Issue:3 Volume:59 Page:553-558
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Han Chongyang,Rush Anthony M.,Dib-Hajj Sulayman D.,Li Song,Xu Zhe,Wang Yun,Tyrrell Lynda,Wang Xiaoliang,Yang Yong,Waxman Stephen G.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

1. Hereditary erythermalgia and acquired erythromelalgia;van Genderen;Am J Med Genet,1993

2. Autosomal dominant erythromelalgia;Finley;Am J Med Genet,1992

3. The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32;Drenth;Am J Hum Genet,2001

4. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia;Yang;J Med Genet,2004

5. Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons;Dib-Hajj;Brain,2005

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