Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease (Q28218346)
Jump to navigation
Jump to search
scientific article (publication date: May 2002)
Language | Label | Description | Also known as |
---|---|---|---|
English | Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease |
scientific article (publication date: May 2002) |
Statements
Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease (English)
0 references
May 2002
0 references
59
0 references
5
0 references
862-5
0 references