Identification of Genes Associated with Familial Focal Segmental Glomerulosclerosis Through Transcriptomics and In Silico Analysis, Including RPL27, TUBB6, and PFDN5

Identification of Genes Associated with Familial Focal Segmental Glomerulosclerosis Through Transcriptomics and In Silico Analysis, Including RPL27, TUBB6, and PFDN5

Focal segmental glomerulosclerosis (FSGS) is a major cause of nephrotic syndrome and often leads to progressive kidney failure. Its varying clinical presentation suggests potential genetic diversity, requiring further molecular investigation. This study aims to elucidate some of the genetic and mole...

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Bibliographic Details
Main Author: Mahmoud, Anfal (author)
Other Authors: Alhamidi, Reem (author), Ilce, Burcu (author), Hamad, Alaa (author), Ali, Nival (author), Mahasneh, Amjad (author), Talaat, Iman (author), Tlili, Abdelaziz (author), Hamoudi, Rifat (author)
Format: article
Published: 2024
Subjects:
Focal Segmental Glomerulosclerosis (FSGS)
Minimal Change Disease (MCD)
Genetic
Glomerular
Tubulointerstitial
Online Access:https://hdl.handle.net/11073/33276
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