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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.
Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.