Disruption of Gen1 Causes Congenital Anomalies of the Kidney and Urinary Tract in Mice

Congenital anomalies of the kidney and urinary tract (CAKUT) are among the most common developmental defects in humans. Despite of several known CAKUT-related loci (HNF1B, PAX2, EYA1, etc.), the genetic etiology of CAKUT remains to be elucidated for most patients. In this study, we report that disru...

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Detalles Bibliográficos
Autores principales: Wang, Herui, Zhang, Chi, Wang, Xiaowen, Lian, Yaru, Guo, Bin, Han, Miao, Zhang, Xiaoe, Zhu, Xiaoting, Xu, Sixian, Guo, Zengli, Bi, Yunli, Shen, Qian, Wang, Xiang, Liu, Jiaojiao, Zhuang, Yuan, Ni, Ting, Xu, Hong, Wu, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821045/
https://www.ncbi.nlm.nih.gov/pubmed/29483821
http://dx.doi.org/10.7150/ijbs.22768

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821045/
https://www.ncbi.nlm.nih.gov/pubmed/29483821
http://dx.doi.org/10.7150/ijbs.22768

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