APOL1-Associated Collapsing Focal Segmental Glomerulosclerosis in a Patient With Stimulator of Interferon Genes (STING)-Associated Vasculopathy With Onset in Infancy (SAVI)-Reference-Cited by-同舟云学术

APOL1-Associated Collapsing Focal Segmental Glomerulosclerosis in a Patient With Stimulator of Interferon Genes (STING)-Associated Vasculopathy With Onset in Infancy (SAVI)

Published:2020-02 Issue:2 Volume:75 Page:287-290
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Abid Qassim,Best Rocha Alejandro,Larsen Christopher P.,Schulert Grant,Marsh Rebecca,Yasin Shima,Patty-Resk Cathy,Valentini Rudolph P.,Adams Matthew,Baracco Rossana

Publisher

Elsevier BV

Subject

Nephrology

Reference19 articles.

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2. Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene;Tzur;Hum Genet,2010

3. Histopathologic findings associated with APOL1 risk variants in chronic kidney disease;Larsen;Mod Pathol,2014

4. Apolipoprotein L1 risk variants associate with systemic lupus erythematosus-associated collapsing glomerulopathy;Larsen;J Am Soc Nephrol,2013

5. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy;Kopp;J Am Soc Nephrol,2011

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