APA引文

Cason, R. K., Williams, A., Chryst-Stangl, M., Wu, G., Huggins, K., Brathwaite, K. E., . . . Gbadegesin, R. A. (2022, July). Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations. Frontiers in Pediatrics.

Chicago Style (17th ed.) Citation

Cason, Rachel K., et al. "Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations." Frontiers in Pediatrics Jul. 2022.

MLA引文

Cason, Rachel K., et al. "Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations." Frontiers in Pediatrics, Jul. 2022.