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Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults.
Elevated Urinary Levels of 8-Hydroxy-2'-deoxyguanosine in a Japanese Child of Xeroderma Pigmentosum/Cockayne Syndrome Complex with Infantile Onset of Nephrotic Syndrome.
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
Twenty-four-year-old male patient with infantile onset of Schimke immuno-osseous dysplasia.