SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
Titel:
SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
Auteur:
Fertleman, Caroline R. Baker, Mark D. Parker, Keith A. Moffatt, Sarah Elmslie, Frances V. Abrahamsen, Bjarke Ostman, Johan Klugbauer, Norbert Wood, John N. Gardiner, R. Mark Rees, Michele