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Genetic basis of human congenital anomalies of the kidney and urinary tract

The clinical spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) encompasses a common birth defect in humans that has significant impact on long-term patient survival. Overall, data indicate that approximately 20% of patients may have a genetic disorder that is usually not detec...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Clin Invest
Päätekijät: Sanna-Cherchi, Simone, Westland, Rik, Ghiggeri, Gian Marco, Gharavi, Ali G.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Clinical Investigation 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5749511/
https://ncbi.nlm.nih.gov/pubmed/29293093
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI95300
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