Cite
MLA Citation
M Chol et al.. “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.” Journal of medical genetics, vol. 40, no. 3, 2003, pp. 188–191. http://access.bl.uk/ark:/81055/vdc_100134878536.0x000042