The role of alpha-actinin-4 in human kidney disease

Mutations in the Alpha-actinin-4 gene (ACTN4) cause a rare form of familial focal segmental glomerulosclerosis in humans. Individuals with kidney disease-associated ACTN4 mutations tend to have mild to moderate proteinuria, with many developing decreased kidney function progressing to end stage kidn...

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Vydáno v:Cell Biosci
Hlavní autoři: Feng, Di, DuMontier, Clark, Pollak, Martin R
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2015
Témata:
Review
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4545552/
https://ncbi.nlm.nih.gov/pubmed/26301083
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13578-015-0036-8
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