The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency. (Q43074243)
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scientific article published in March 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency. |
scientific article published in March 2003 |
Statements
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency (English)
M Chol
S Lebon
P Bénit
D Chretien
P de Lonlay
A Goldenberg
S Odent
C Vincent-Delorme
P Rustin
A Rötig