Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late‐onset disorder of mitochondrial DNA maintenance

MLA

Francesco Bruni, et al. “Identification of a Novel Heterozygous Guanosine Monophosphate Reductase (GMPR) Variant in a Patient with a Late‐onset Disorder of Mitochondrial DNA Maintenance.” Clinical Genetics, vol. 97, Nov. 2019, pp. 276–86. EBSCOhost, https://doi.org/10.1111/cge.13652.

APA

Francesco Bruni, Kyle Thompson, Grainne S. Gorman, Ewen W. Sommerville, Ilaria Dalla Rosa, Robert W. Taylor, Patrick F. Chinnery, Andrew M. Schaefer, Patrick Yu-Wai-Man, Masha M. Rosenberg, Mariana C. Rocha, Lizbeth Hedstrom, Langping He, Gavin Falkous, Emma L. Blakely, & Antonella Spinazzola. (2019). Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late‐onset disorder of mitochondrial DNA maintenance. Clinical Genetics, 97, 276–286. https://doi.org/10.1111/cge.13652

Chicago

Francesco Bruni, Kyle Thompson, Grainne S. Gorman, Ewen W. Sommerville, Ilaria Dalla Rosa, Robert W. Taylor, Patrick F. Chinnery, et al. 2019. “Identification of a Novel Heterozygous Guanosine Monophosphate Reductase (GMPR) Variant in a Patient with a Late‐onset Disorder of Mitochondrial DNA Maintenance.” Clinical Genetics 97 (November): 276–86. doi:10.1111/cge.13652.