Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations

Cason, R. K., Williams, A., Chryst-Stangl, M., Wu, G., Huggins, K., Brathwaite, K. E., Lane, B. M., Greenbaum, L. A., D’Agati, V. D., & Gbadegesin, R. A. (2022). 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, 10. https://doi.org/10.3389/fped.2022.915174

Authors:

Rachel K. Cason

Anna E. Williams

Megan Chryst-Stangl

Guanghong Wu

Kinsie Huggins

Kaye E. Brathwaite

Brandon M. Lane

Larry A. Greenbaum

Vivette D. D’Agati

Rasheed Gbadegesin

Affiliated Authors: