Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.


ATMIŞ B., ATMIŞ A., YARALI O., ESMERAY ŞENOL P., Gemici A.

51st Annual ESPN Meeting, 3 - 06 October 2018, vol.33

  • Publication Type: Conference Paper / Summary Text
  • Volume: 33
  • Çukurova University Affiliated: Yes