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Nephronophthisis

Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease, which represents the most frequent genetic cause for end-stage renal disease up to the third decade of life. Nephronophthisis is caused by mutations in eleven different genes called nephrocystins (NPHP1-11, NPHP1L). With an inc...

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Bibliografske podrobnosti
Main Authors: Wolf, Matthias T. F., Hildebrandt, Friedhelm
Format: Artigo
Jezik:Inglês
Izdano: 2010
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4160028/
https://ncbi.nlm.nih.gov/pubmed/20652329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-010-1585-z
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