(Q28218346)

English

Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease

scientific article (publication date: May 2002)

In more languages
default for all languages
No label defined

No description defined

Statements

Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease (English)
0 references
0 references
0 references
Leonardo Salviati
0 references
Minerva M Rasalan
0 references
David F Kronn
0 references
Alex Braun
0 references
Peter Canoll
0 references
Mercy Davidson
0 references
Sara Shanske
0 references
Eduardo Bonilla
0 references
Arthur P Hays
0 references
Eric A Schon
0 references
May 2002
0 references
59
0 references
5
0 references
862-5
0 references

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit