اسماعیلی چمگردانی, لیلا

[ 1 ] - تعیین ژنوتیپ مارکر rs2274625 در ژن NPHS2 مرتبط با سندروم نفروتیک در جمعیت اصفهان

Introduction: Nephrotic syndrome (NS) is a genetic disease belonging to a heterogeneous group of glomerular disorders, which mainly occurs within the children. Linkage analysis using single nucleotide polymorphisms (SNP) is used as an indirect method in molecular diagnosis of the disease. A large number of SNP markers have been introduced in NPHS2gene in the available electronic databases. M...