Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I.

MLA

Rawa, Katarzyna, et al. “Characterization of a Novel Mutation in the NADH-Cytochrome B5 Reductase Gene Responsible for Rare Hereditary Methaemoglobinaemia Type I.” Acta Haematologica, vol. 130, no. 2, 2013, pp. 122–25. EBSCOhost, https://doi.org/10.1159/000347041.

APA

Rawa, K., Chelmecka-Hanusiewicz, L., Plochocka, D., Pawinska-Wasikowska, K., Balwierz, W., & Burzynska, B. (2013). Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I. Acta Haematologica, 130(2), 122–125. https://doi.org/10.1159/000347041

Chicago

Rawa, Katarzyna, Liliana Chelmecka-Hanusiewicz, Danuta Plochocka, Katarzyna Pawinska-Wasikowska, Walentyna Balwierz, and Beata Burzynska. 2013. “Characterization of a Novel Mutation in the NADH-Cytochrome B5 Reductase Gene Responsible for Rare Hereditary Methaemoglobinaemia Type I.” Acta Haematologica 130 (2): 122–25. doi:10.1159/000347041.