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Loss of polycystin-1 causes centrosome amplification and genomic instability

Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenetic disease predominantly caused by alteration or dysregulation of the PKD1 gene, which encodes polycystin-1 (PC1). The disease is characterized by the progressive expansion of bilateral fluid-filled renal cysts that ult...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Battini, Lorenzo, Macip, Salvador, Fedorova, Elena, Dikman, Steven, Somlo, Stefan, Montagna, Cristina, Gusella, G. Luca
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2008
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2722891/
https://ncbi.nlm.nih.gov/pubmed/18566106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn180
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