APA (7th ed.) Citation

Kirschner, M., Heinen, I. R., Koschmieder, S., Manco, L., Bento, C., Eggermann, T., . . . Fuchs, R. (2022). Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling. Clinical Case Reports, 10(3), 1. https://doi.org/10.1002/ccr3.5501

Chicago Style (17th ed.) Citation

Kirschner, Martin, et al. "Novel Homozygous Nonsense Mutation in the P5′N‐1 Coding Gene as an Alternative Cause for Hereditary Anemia with Basophilic Stippling." Clinical Case Reports 10, no. 3 (2022): 1. https://doi.org/10.1002/ccr3.5501.

MLA (9th ed.) Citation

Kirschner, Martin, et al. "Novel Homozygous Nonsense Mutation in the P5′N‐1 Coding Gene as an Alternative Cause for Hereditary Anemia with Basophilic Stippling." Clinical Case Reports, vol. 10, no. 3, 2022, p. 1, https://doi.org/10.1002/ccr3.5501.