SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
Top Cited Papers
- 1 December 2006
- Vol. 52 (5) , 767-774
- https://doi.org/10.1016/j.neuron.2006.10.006
Abstract
No abstract availableKeywords
Funding Information
- Wellcome Trust
- Medical Research Council
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