Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
Resource Type
Article
Authors
Martino, Jeremiah ; Liu, Qingxue ; Vukojevic, Katarina ; Ke, Juntao ; Lim, Tze Y. ; Khan, Atlas ; Gupta, Yask ; Perez, Alejandra ; Yan, Zonghai ; Milo Rasouly, Hila ; Vena, Natalie ; Lippa, Natalie ; Giordano, Jessica L. ; Saraga, Marijan ; Saraga-Babic, Mirna ; Westland, Rik ; Bodria, Monica ; Piaggio, Giorgio ; Bendapudi, Pavan K. ; Iglesias, Alejandro D. ; Wapner, Ronald J. ; Tasic, Velibor ; Wang, Fan ; Ionita-Laza, Iuliana ; Ghiggeri, Gian Marco ; Kiryluk, Krzysztof ; Sampogna, Rosemary V. ; Mendelsohn, Cathy L. ; D’Agati, Vivette D. ; Gharavi, Ali G. ; Sanna-Cherchi, Simone
Source
In Genetics in Medicine December 2023 25(12)
Subject
Language
ISSN
1098-3600