Cite
Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia.
MLA
Grabowska, Dorota, et al. “Compound Heterozygosity of Two Missense Mutations in the NADH-Cytochrome B5 Reductase Gene of a Polish Patient with Type I Recessive Congenital Methaemoglobinaemia.” European Journal of Haematology, vol. 70, no. 6, June 2003, pp. 404–09. EBSCOhost, https://doi.org/10.1034/j.1600-0609.2003.00070.x.
APA
Grabowska, D., Plochocka, D., Jablonska-Skwiecinska, E., Chelstowska, A., Lewandowska, I., Staniszewska, K., Majewska, Z., Witos, I., & Burzynska, B. (2003). Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia. European Journal of Haematology, 70(6), 404–409. https://doi.org/10.1034/j.1600-0609.2003.00070.x
Chicago
Grabowska, Dorota, Danuta Plochocka, Ewa Jablonska-Skwiecinska, Anna Chelstowska, Irmina Lewandowska, Krystyna Staniszewska, Zofia Majewska, Iwona Witos, and Beata Burzynska. 2003. “Compound Heterozygosity of Two Missense Mutations in the NADH-Cytochrome B5 Reductase Gene of a Polish Patient with Type I Recessive Congenital Methaemoglobinaemia.” European Journal of Haematology 70 (6): 404–9. doi:10.1034/j.1600-0609.2003.00070.x.