Familial episodic limb pain in kindreds with novel Nav1.9 mutations
Author:
Funder
Japan Society for the Promotion of Science
AMED
Japan Society for the Promotion of Science (JP)
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference47 articles.
1. Gain-of-function mutations in SCN11A cause familial episodic pain;XY Zhang;Am J Hum Genet,2013
2. Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant;E Leipold;Nat Commun,2015
3. Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families;H Okuda;PLoS One,2016
4. NaV1.9: a sodium channel linked to human pain;SD Dib-Hajj;Nat Rev Neurosci,2015
5. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia;Y Yang;J Med Genet,2004
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