Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism

BACKGROUND: Congenital anomalies of the kidney and urinary tract (CAKUT), such as renal dysplasia, hydronephrosis, or vesicoureteral reflux, are the most common causes of end-stage renal disease. However, the genetic etiology of CAKUT remains unclear. In this study, we performed whole exome sequenci...

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Pubblicato in:BMC Urol
Autori principali: Mizuno, Kentaro, Nakane, Akihiro, Nishio, Hidenori, Moritoki, Yoshinobu, Kamisawa, Hideyuki, Kurokawa, Satoshi, Kato, Taiki, Ando, Ryosuke, Maruyama, Tetsuji, Yasui, Takahiro, Hayashi, Yutaro
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2017
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5712187/
https://ncbi.nlm.nih.gov/pubmed/29197384
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12894-017-0300-9
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