The Role of p.Ser1105Ser (in <i>NPHS1</i> Gene) and p.Arg548Leu (in <i>PLCE1</i> Gene) with Disease Status of Vietnamese Patients with Congenital Nephrotic Syndrome: Benign or Pathogenic?
<i>Background and Objectives</i>: Congenital nephrotic syndrome (CNS), a genetic disease caused by mutations in genes on autosomes, usually occurs in the first three months after birth. A number of genetic mutations in genes, which encode for the components of the glomerular filtration b...
Main Authors: | Nguyen Thi Kim Lien, Pham Van Dem, Nguyen Thu Huong, Tran Minh Dien, Ta Thi Thu Thuy, Nguyen Van Tung, Nguyen Huy Hoang, Nguyen Thi Quynh Huong |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2019-04-01
|
Series: | Medicina |
Subjects: | |
Online Access: | https://www.mdpi.com/1010-660X/55/4/102 |
Similar Items
-
Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome
by: Aiysha Abid, et al.
Published: (2018-06-01) -
Genetic Association Studies of <i>MICB</i> and <i>PLCE1</i> with Severity of Dengue in Indonesian and Taiwanese Populations
by: Imaniar Noor Faridah, et al.
Published: (2023-11-01) -
Relation between single nucleotide polymorphism rs3738423 (C>T) of NPHS2 gene and some biochemical parameters in pediatrics nephrotic syndrome patients
by: Nga Van Vu, et al.
Published: (2019-11-01) -
<i>Verticillium dahliae VdPBP1</i> Transcription Factor Is Required for Hyphal Growth, Virulence, and Microsclerotia Formation
by: Huong Thi Nguyen, et al.
Published: (2024-01-01) -
Nephrin and podocin mRNA detection in urine sediment of dogs with chronic kidney disease: preliminary observations
by: Souza Camilla de, et al.
Published: (2022-04-01)