A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia (Q79412625)
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scientific article published on 01 January 2007
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia |
scientific article published on 01 January 2007 |
Statements
A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia (English)
Emmanuelle Sarzi
Michael D Brown
Sophie Lebon
Dominique Chretien
Arnold Munnich
1 January 2007