APA (7th ed.) Citation

Matilainen, S., Carroll, C. J., Richter, U., Euro, L., Pohjanpelto, M., Paetau, A., . . . Suomalainen, A. (2017). Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome. Human molecular genetics, 26(17), 3352-3361. https://doi.org/10.1093/hmg/ddx221

Chicago Style (17th ed.) Citation

Matilainen, Sanna, Christopher J. Carroll, Uwe Richter, Liliya Euro, Max Pohjanpelto, Anders Paetau, Pirjo Isohanni, and Anu Suomalainen. "Defective Mitochondrial RNA Processing Due to PNPT1 Variants Causes Leigh Syndrome." Human Molecular Genetics 26, no. 17 (2017): 3352-3361. https://doi.org/10.1093/hmg/ddx221.

MLA (9th ed.) Citation

Matilainen, Sanna, et al. "Defective Mitochondrial RNA Processing Due to PNPT1 Variants Causes Leigh Syndrome." Human Molecular Genetics, vol. 26, no. 17, 2017, pp. 3352-3361, https://doi.org/10.1093/hmg/ddx221.