Cargando…
Nephronophthisis: A review of genotype–phenotype correlation
Nephronophthisis is an autosomal recessive cystic kidney disease and one of the most common genetic disorders causing end‐stage renal disease in children. Nephronophthisis is a genetically heterogenous disorder with more than 25 identified genes. In 10%–20% of cases, there are additional features of...
Autores principales: | Luo, Fenglan, Tao, Yu‐Hong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175366/ https://www.ncbi.nlm.nih.gov/pubmed/29717526 http://dx.doi.org/10.1111/nep.13393 |
Ejemplares similares
-
Nephronophthisis
por: Salomon, Rémi, et al.
Publicado: (2008) -
Nephronophthisis: A Genetically Diverse Ciliopathy
por: Simms, Roslyn J., et al.
Publicado: (2011) -
The Role of Centrosome Distal Appendage Proteins (DAPs) in Nephronophthisis and Ciliogenesis
por: Mansour, Fatma, et al.
Publicado: (2021) -
Alteration of nephrocystins and IFT-A proteins causes similar ciliary phenotypes leading to Nephronophthisis
por: Saunier, S, et al.
Publicado: (2012) -
Nephronophthisis-Pathobiology and Molecular Pathogenesis of a Rare Kidney Genetic Disease
por: Gupta, Shabarni, et al.
Publicado: (2021)