[go: up one dir, main page]

(Q28245708)

English

Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations

scientific article (publication date: 1994)

In more languages
default for all languages
No label defined

No description defined

Statements

Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations (English)
0 references
E Plassart
0 references
J Reboul
0 references
C S Rime
0 references
D Recan
0 references
P Millasseau
0 references
B Eymard
0 references
J Pelletier
0 references
C Thomas
0 references
F Chapon
0 references
C Desnuelle
0 references
1994
0 references
2
0 references
2
0 references
110-24
0 references

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit