The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood.

MLA

Thomasová, Dana, et al. “The Most Common Founder Pathogenic Variant c.868G > A (p.Val290Met) in the NPHS2 Gene in a Representative Adult Czech Cohort with Focal Segmental Glomerulosclerosis Is Associated with a Milder Disease and Its Underdiagnosis in Childhood.” Frontiers in Medicine, vol. 10, Dec. 2023, p. 1320054. EBSCOhost, https://doi.org/10.3389/fmed.2023.1320054.

APA

Thomasová, D., Zelinová, M., Libik, M., Geryk, J., Votýpka, P., Rajnochová Bloudíčková, S., Krejčí, K., Reiterová, J., Jančová, E., Machová, J., Kollárová, M., Rychík, I., Havrda, M., Horáčková, M., Putzová, M., Šafránek, R., Kollár, M., & Macek, M., Jr. (2023). The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood. Frontiers in Medicine, 10, 1320054. https://doi.org/10.3389/fmed.2023.1320054

Chicago

Thomasová, Dana, Michaela Zelinová, Malgorzata Libik, Jan Geryk, Pavel Votýpka, Silvie Rajnochová Bloudíčková, Karel Krejčí, et al. 2023. “The Most Common Founder Pathogenic Variant c.868G > A (p.Val290Met) in the NPHS2 Gene in a Representative Adult Czech Cohort with Focal Segmental Glomerulosclerosis Is Associated with a Milder Disease and Its Underdiagnosis in Childhood.” Frontiers in Medicine 10 (December): 1320054. doi:10.3389/fmed.2023.1320054.