Kamps, R., Szklarczyk, R., Theunissen, T. E., Hellebrekers, D. M. E. I., Sallevelt, S. C. E. H., Boesten, I. B., . . . Smeets, H. J. M. (2018). Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease. Eur J Hum Genet.
Citação norma ChicagoKamps, Rick, et al. "Genetic Defects in MtDNA-encoded Protein Translation Cause Pediatric, Mitochondrial Cardiomyopathy With Early-onset Brain Disease." Eur J Hum Genet 2018.
MLA CitationKamps, Rick, et al. "Genetic Defects in MtDNA-encoded Protein Translation Cause Pediatric, Mitochondrial Cardiomyopathy With Early-onset Brain Disease." Eur J Hum Genet 2018.
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