Cite
PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants.
MLA
Maciak, Karolina, et al. “PKLR Mutations in Pyruvate Kinase Deficient Polish Patients: Functional Characteristics of c.101-1G > A and c.1058delAAG Variants.” Blood Cells, Molecules & Diseases, vol. 107, July 2024, p. 102841. EBSCOhost, https://doi.org/10.1016/j.bcmd.2024.102841.
APA
Maciak, K., Jurkiewicz, A., Strojny, W., Adamowicz-Salach, A., Romiszewska, M., Jackowska, T., Kwiecinska, K., Poznanski, J., Gora, M., & Burzynska, B. (2024). PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants. Blood Cells, Molecules & Diseases, 107, 102841. https://doi.org/10.1016/j.bcmd.2024.102841
Chicago
Maciak, Karolina, Aneta Jurkiewicz, Wojciech Strojny, Anna Adamowicz-Salach, Magdalena Romiszewska, Teresa Jackowska, Kinga Kwiecinska, Jaroslaw Poznanski, Monika Gora, and Beata Burzynska. 2024. “PKLR Mutations in Pyruvate Kinase Deficient Polish Patients: Functional Characteristics of c.101-1G > A and c.1058delAAG Variants.” Blood Cells, Molecules & Diseases 107 (July): 102841. doi:10.1016/j.bcmd.2024.102841.