SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
Neuron2006Vol. 52(5), pp. 767–774
Citations Over TimeTop 1% of 2006 papers
Caroline Fertleman, Mark D. Baker, Keith A. Parker, S. Louise Moffatt, Frances Elmslie, Bjarke Abrahamsen, Johan Östman, Norbert Klugbauer, John N. Wood, R. Mark Gardiner, Michele Rees
Related Papers
- → Painful Na-channelopathies: an expanding universe(2013)76 cited
- → Erythromelalgia: A hereditary pain syndrome enters the molecular era(2005)86 cited
- → SCN10A Mutation in a Patient with Erythromelalgia Enhances C-Fiber Activity Dependent Slowing(2016)52 cited
- [Channelopathy of voltage-gated sodium channel].(1999)
- Channelopathy of Voltage gated Sodium Channel(1999)