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Komulainen T, Hautakangas MR, Hinttala R, et al. Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes. JIMD Rep. 2015;23:91-100doi: 10.1007/8904_2015_438.
Komulainen, T., Hautakangas, M. R., Hinttala, R., Pakanen, S., Vähäsarja, V., Lehenkari, P., Olsen, P., Vieira, P., Saarenpää-Heikkilä, O., Palmio, J., Tuominen, H., Kinnunen, P., Majamaa, K., Rantala, H., & Uusimaa, J. (2015). Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes. JIMD reports, 2391-100. https://doi.org/10.1007/8904_2015_438
Komulainen, Tuomas, et al. "Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes." JIMD reports vol. 23 (2015): 91-100. doi: https://doi.org/10.1007/8904_2015_438
Komulainen T, Hautakangas MR, Hinttala R, Pakanen S, Vähäsarja V, Lehenkari P, Olsen P, Vieira P, Saarenpää-Heikkilä O, Palmio J, Tuominen H, Kinnunen P, Majamaa K, Rantala H, Uusimaa J. Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes. JIMD Rep. 2015;23:91-100. doi: 10.1007/8904_2015_438. Epub 2015 May 05. PMID: 25940035; PMCID: PMC4484910.
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