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APA Citation
Lebon, S., Chol, M., Benit, P., Mugnier, C., Chretien, D., Giurgea, I., Kern, I., Girardin, E., Hertz-Pannier, L., de Lonlay, P., Rötig, A., Rustin, P., & Munnich, A. (2003). recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency. Journal of medical genetics, 40(12), 896–899. http://access.bl.uk/ark:/81055/vdc_100135138864.0x000031