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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التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Mahmoud, Anfal (author)
مؤلفون آخرون:	Alhamidi, Reem (author), Ilce, Burcu (author), Hamad, Alaa (author), Ali, Nival (author), Mahasneh, Amjad (author), Talaat, Iman (author), Tlili, Abdelaziz (author), Hamoudi, Rifat (author)
التنسيق:	article
منشور في:	2024
الموضوعات:	Focal Segmental Glomerulosclerosis (FSGS) Minimal Change Disease (MCD) Genetic Glomerular Tubulointerstitial
الوصول للمادة أونلاين:	https://hdl.handle.net/11073/33276
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Identification of Genes Associated with Familial Focal Segmental Glomerulosclerosis Through Transcriptomics and In Silico Analysis, Including RPL27, TUBB6, and PFDN5

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