Abdelhakim, A. H., Dharmadhikari, A. V., Ragi, S. D., Carvalho, J. R. L. d., Xu, C. L., Thomas, A. L., . . . Tsang, S. H. (2020). Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency. Orphanet Journal of Rare Diseases, 15(1), 1. https://doi.org/10.1186/s13023-020-01600-8
Chicago-referens (17:e uppl.)Abdelhakim, Aliaa H., et al. "Compound Heterozygous Inheritance of Two Novel COQ2 Variants Results in Familial Coenzyme Q Deficiency." Orphanet Journal of Rare Diseases 15, no. 1 (2020): 1. https://doi.org/10.1186/s13023-020-01600-8.
MLA-referens (9:e uppl.)Abdelhakim, Aliaa H., et al. "Compound Heterozygous Inheritance of Two Novel COQ2 Variants Results in Familial Coenzyme Q Deficiency." Orphanet Journal of Rare Diseases, vol. 15, no. 1, 2020, p. 1, https://doi.org/10.1186/s13023-020-01600-8.
