NPHS2 mutations account for only 15% of Nephrotic Syndrome cases
Detection and functional characterization of genetic mutations in familial and sp...
Whole Exome Sequencing in Brazilian Children and Adolescents with Steroid Resistan...
EEstablishment of Exome Sequencing as a Resarch Tool for Screening Genes Related t...
Epidemiology of pediatric nephrotic syndrome in Brazil: incidence, prevalence, res...
Occurrence, diversity and molecular pathogenicity of avian coronavirus in quail
MOLECULAR EVALUATION OF VARIANTS IN RELATION TO THE RISK OF DEVELOPING STEROID-SEN...