(Q28118877)

English

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes

scientific journal article

Statements

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes (English)
Caroline R. Fertleman
Mark D. Baker
Keith A. Parker
Sarah Moffatt
Frances V. Elmslie
Bjarke Abrahamsen
Johan Ostman
John N. Wood
R. Mark Gardiner
Michele Rees
7 December 2006
767–774

Identifiers

 
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