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

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作者： Rachel K,Cason ^[1] ; Anna,Williams ^[1] ; Megan,Chryst-Stangl ^[1] ; Guanghong,Wu ^[1] ; Kinsie,Huggins ^[1] ; Kaye E,Brathwaite ^[2] ; Brandon M,Lane ^[1] ; Larry A,Greenbaum ^[3] ; Vivette D,D'Agati ^[4] ; Rasheed A,Gbadegesin ^[1]

作者单位： Division of Nephrology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States. ^[1] Division of Pediatric Nephrology, Children's Hospital at Montefiore, The Bronx, NY, United States. ^[2] Division of Pediatric Nephrology, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, United States. ^[3] Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, United States. ^[4]

关键词 APOL1 collapsing FSGS focal segmental glomerulosclerosis nephrotic syndrome nucleoporin genes

DOI 10.3389/fped.2022.915174

PMID 35874595

发布时间 2022-07-26

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Frontiers in pediatrics

2022年10卷

915174页

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

Frontiers in pediatrics

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Frontiers in pediatrics

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

Frontiers in pediatrics

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Frontiers in pediatrics

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