(Q28118877)

English

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

scientific journal article

In more languages
default for all languages
No label defined

No description defined

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

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit